FDA 510(k)

STERIL.WRAP(#221901,2,3,4,5,6,7,8,9)

K-Number: K760662 · 1976-12-30

Decision Date1976-12-30

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERIL.WRAP(#221901,2,3,4,5,6,7,8,9) is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K760662. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERIL.WRAP(#221901,2,3,4,5,6,7,8,9)?

STERIL.WRAP(#221901,2,3,4,5,6,7,8,9) is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760662.

When did STERIL.WRAP(#221901,2,3,4,5,6,7,8,9) receive FDA 510(k) clearance?

STERIL.WRAP(#221901,2,3,4,5,6,7,8,9) received FDA 510(k) clearance on 1976-12-30, under 510(k) number K760662.

Who is the listed applicant for STERIL.WRAP(#221901,2,3,4,5,6,7,8,9)?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERIL.WRAP(#221901,2,3,4,5,6,7,8,9)?

The FDA product code for STERIL.WRAP(#221901,2,3,4,5,6,7,8,9) is FRG.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.