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FDA 510(k)

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS

K-Number: K910196 · 1991-03-27

ApplicantC.R. Bard, Inc.
Decision Date1991-03-27
Product CodeFGH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS 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 1991-03-27 under 510(k) number K910196. The device is classified under product code FGH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS?

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS is a medical device that received FDA 510(k) clearance on 1991-03-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K910196.

When did BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS receive FDA 510(k) clearance?

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS received FDA 510(k) clearance on 1991-03-27, under 510(k) number K910196.

Who is the listed applicant for BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS?

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 HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS?

The FDA product code for BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS is FGH.

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Other records listing C.R. Bard, Inc. as applicant

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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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