THE RECLASSIFICATION PETITION ALLOWS
MANUFACTURERS AND OTHERS TO REQUE CHANGE IN THE REGULATORY CONTROL
CATEGORY (CLASS) OF MEDICAL DEVICES. THE PETITIONS MUST PROVIDE
ADEQUATE INFORMATION TO DEMONSTRATE THAT TH REQUESTED CHANGE WILL
PROVIDE OR IS NECESSARY TO PROVIDE REASONABLE ASSURANCE OF SAFETY
AND EFFECTIVENESS OF THE DEVICE.
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.