FDA 510(k)

BARD URODYNAMIC CATHETER

K-Number: K924714 · 1993-09-21

Decision Date1993-09-21

Product CodeFEN

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD URODYNAMIC 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 1993-09-21 under 510(k) number K924714. The device is classified under product code FEN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD URODYNAMIC CATHETER?

BARD URODYNAMIC CATHETER is a medical device that received FDA 510(k) clearance on 1993-09-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K924714.

When did BARD URODYNAMIC CATHETER receive FDA 510(k) clearance?

BARD URODYNAMIC CATHETER received FDA 510(k) clearance on 1993-09-21, under 510(k) number K924714.

Who is the listed applicant for BARD URODYNAMIC 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 BARD URODYNAMIC CATHETER?

The FDA product code for BARD URODYNAMIC CATHETER is FEN.

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

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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.