This information
collection is approved through 12/93. The final medic device
regulations will likely be promulgated within the next six months.
When final rules are published, OMB expects that FDA will wor
expeditiously to withdraw from its involvement in the National
Cardiac Pacemaker Registry.
Inventory as of this Action
Requested
Previously Approved
12/31/1993
12/31/1993
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THIS COLLECTION WI COLLECT INFORMATION
FROM PHYSICIANS AND PROVIDERS WHO PERFORM MEDICARE COVERED
PACEMAKER PROCEDURES. THE INFORMATION IS FOR THE CONGRESSIONALLY
MANDATED PACEMAKER REGISTRY.
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.