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FDA 510(k)

UNDER BOTTOCKS DRAPE

K-Number: K760997 · 1977-03-23

ApplicantC.R. Bard, Inc.
Decision Date1977-03-23
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UNDER BOTTOCKS DRAPE 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 1977-03-23 under 510(k) number K760997. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNDER BOTTOCKS DRAPE?

UNDER BOTTOCKS DRAPE is a medical device that received FDA 510(k) clearance on 1977-03-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760997.

When did UNDER BOTTOCKS DRAPE receive FDA 510(k) clearance?

UNDER BOTTOCKS DRAPE received FDA 510(k) clearance on 1977-03-23, under 510(k) number K760997.

Who is the listed applicant for UNDER BOTTOCKS DRAPE?

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 UNDER BOTTOCKS DRAPE?

The FDA product code for UNDER BOTTOCKS DRAPE is KKX.

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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.

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