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FDA 510(k)

TRAY, FOLEY CATHETER

K-Number: K760254 · 1976-08-23

ApplicantC.R. Bard, Inc.
Decision Date1976-08-23
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRAY, FOLEY CATHETER 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 1976-08-23 under 510(k) number K760254. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY, FOLEY CATHETER?

TRAY, FOLEY CATHETER is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760254.

When did TRAY, FOLEY CATHETER receive FDA 510(k) clearance?

TRAY, FOLEY CATHETER received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760254.

Who is the listed applicant for TRAY, FOLEY CATHETER?

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 TRAY, FOLEY CATHETER?

The FDA product code for TRAY, FOLEY CATHETER is GBM.

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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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