FDA 510(k)

BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF

K-Number: K910846 · 1991-08-16

Decision Date1991-08-16

Product CodeEZC

Advisory CommitteeGU

DecisionUnknown

Device Summary

BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF 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 1991-08-16 under 510(k) number K910846. The device is classified under product code EZC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF?

BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF is a medical device that received FDA 510(k) clearance on 1991-08-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K910846.

When did BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF receive FDA 510(k) clearance?

BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF received FDA 510(k) clearance on 1991-08-16, under 510(k) number K910846.

Who is the listed applicant for BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF?

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 LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF?

The FDA product code for BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIF is EZC.

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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.