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FDA 510(k)

BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY

K-Number: K922527 · 1994-04-14

ApplicantC.R. Bard, Inc.
Decision Date1994-04-14
Product CodeKOD
Advisory CommitteeGU
DecisionUnknown

Device Summary

BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY 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 1994-04-14 under 510(k) number K922527. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY?

BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1994-04-14. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K922527.

When did BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY receive FDA 510(k) clearance?

BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY received FDA 510(k) clearance on 1994-04-14, under 510(k) number K922527.

Who is the listed applicant for BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY?

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 CATHETERIZATION PROCEDURE TRAY?

The FDA product code for BARD URODYNAMIC CATHETERIZATION PROCEDURE TRAY is KOD.

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Related Devices (Code: KOD)

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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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