FDA 510(k)

BARD ENDOSCOPIC OVERTUBE (#000307)

K-Number: K973500 · 1997-10-16

Decision Date1997-10-16

Product CodeFED

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD ENDOSCOPIC OVERTUBE (#000307) 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 1997-10-16 under 510(k) number K973500. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ENDOSCOPIC OVERTUBE (#000307)?

BARD ENDOSCOPIC OVERTUBE (#000307) is a medical device that received FDA 510(k) clearance on 1997-10-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K973500.

When did BARD ENDOSCOPIC OVERTUBE (#000307) receive FDA 510(k) clearance?

BARD ENDOSCOPIC OVERTUBE (#000307) received FDA 510(k) clearance on 1997-10-16, under 510(k) number K973500.

Who is the listed applicant for BARD ENDOSCOPIC OVERTUBE (#000307)?

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 BARD ENDOSCOPIC OVERTUBE (#000307)?

The FDA product code for BARD ENDOSCOPIC OVERTUBE (#000307) is FED.

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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.