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FCC 18-167 (2018 Order), which eliminated unnecessary and outdated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 Commission’s 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 Commission’s 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
Commission’s 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
Commission’s hearing aid compatibility provisions.
The revisions to the currently
approved information collection are a direct result of the
Commission’s 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 manufacturers’
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 manufacturers’
burden. Service providers’ 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.