FDA 510(k)

BARD FLEXIBLE TIP URETERAL CATHETER

K-Number: K950300 · 1995-04-27

Decision Date1995-04-27

Product CodeEYB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD FLEXIBLE TIP URETERAL 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 1995-04-27 under 510(k) number K950300. The device is classified under product code EYB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD FLEXIBLE TIP URETERAL CATHETER?

BARD FLEXIBLE TIP URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 1995-04-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K950300.

When did BARD FLEXIBLE TIP URETERAL CATHETER receive FDA 510(k) clearance?

BARD FLEXIBLE TIP URETERAL CATHETER received FDA 510(k) clearance on 1995-04-27, under 510(k) number K950300.

Who is the listed applicant for BARD FLEXIBLE TIP URETERAL 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 FLEXIBLE TIP URETERAL CATHETER?

The FDA product code for BARD FLEXIBLE TIP URETERAL CATHETER is EYB.

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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.