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FDA 510(k)

ENDOSCOPE, UROLOGICAL, FEMALE

K-Number: K770943 · 1977-10-18

ApplicantC.R. Bard, Inc.
Decision Date1977-10-18
Product CodeFAL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE, UROLOGICAL, FEMALE 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 1977-10-18 under 510(k) number K770943. The device is classified under product code FAL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPE, UROLOGICAL, FEMALE?

ENDOSCOPE, UROLOGICAL, FEMALE is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K770943.

When did ENDOSCOPE, UROLOGICAL, FEMALE receive FDA 510(k) clearance?

ENDOSCOPE, UROLOGICAL, FEMALE received FDA 510(k) clearance on 1977-10-18, under 510(k) number K770943.

Who is the listed applicant for ENDOSCOPE, UROLOGICAL, FEMALE?

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 ENDOSCOPE, UROLOGICAL, FEMALE?

The FDA product code for ENDOSCOPE, UROLOGICAL, FEMALE is FAL.

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Official Source

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

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