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FDA 510(k)

BARD 4-WIRE URETEROSCOPIC STONE

K-Number: K921233 · 1992-04-27

ApplicantC.R. Bard, Inc.
Decision Date1992-04-27
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD 4-WIRE URETEROSCOPIC STONE 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 1992-04-27 under 510(k) number K921233. The device is classified under product code FFL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD 4-WIRE URETEROSCOPIC STONE?

BARD 4-WIRE URETEROSCOPIC STONE is a medical device that received FDA 510(k) clearance on 1992-04-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K921233.

When did BARD 4-WIRE URETEROSCOPIC STONE receive FDA 510(k) clearance?

BARD 4-WIRE URETEROSCOPIC STONE received FDA 510(k) clearance on 1992-04-27, under 510(k) number K921233.

Who is the listed applicant for BARD 4-WIRE URETEROSCOPIC STONE?

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 4-WIRE URETEROSCOPIC STONE?

The FDA product code for BARD 4-WIRE URETEROSCOPIC STONE is FFL.

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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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