The Commission is requesting a revision to its currently approved hearing aid compatibility information collection that applies to wireless wireless service providers. The revision is necessary to implement the final rules promulgated in the 2018 Report and Order in WT Docket No. 17-228, FCC 18-167 (2018 Order), which eliminated unnecessary and outdated information collection requirements for wireless service providers and replaced these requirements for service providers with a revised web site posting and record retention requirement and a streamlined annual certification requirement. The 2018 Order did not make changes to the currently approved reporting requirements for device manufacturers.
The Commissionâs previous hearing aid compatibility reporting requirements for service providers were intended to provide the Commission with a way to verify compliance with rules requiring service providers to offer specified numbers of hearing aid-compatible handset models, to monitor the status of hearing aid-compatible handset deployment in the marketplace, and to ensure that consumers have access to information about the handset models that serve their needs. The Commissionâs revised and enhanced web site posting, record retention, and annual certification requirements for service providers are an improved means of promoting those goals. The Commission now seeks approval for new FCC Form 855 and its instructions which will be used to ensure that service providers are in compliance with the Commissionâs hearing aid compatibility provisions.
To implement the changes made by the 2018 Order, the Commission modified the FCC Form 655 and its instructions for manufacturers. These non-substantive changes to FCC Form 655 and its instructions were already approved by OMB. The Form 655 and its instructions have been modified to eliminate references to wireless service providers. FCC Form 655 will only be used by device manufacturers on a going forward basis to ensure their compliance with the Commissionâs hearing aid compatibility provisions.
The revisions to the currently approved information collection are a direct result of the Commissionâs actions in the 2018 Order. These revisions represent program changes and are not adjustments. As explained above, the Commission made changes to the reporting burden for service providers but did not make any changes to device manufacturersâ burden. Specifically, the Commission adopted an enhanced web site posting requirement for service providers, a record retention requirement, and a new certification requirement that replaces a much more burdensome reporting requirement. As explained above, the Commission has not made any changes to device manufacturersâ burden. Service providersâ burden related to standards development and labeling requirements also remain unchanged. The Commission estimates that there will be no change in the total of number of respondents and annual responses. However, the annual burden hours have increased by 909 hours.
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.