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FDA 510(k)

LAPAROSCOPY SCISSORS

K-Number: K915544 · 1992-03-09

ApplicantC.R. Bard, Inc.
Decision Date1992-03-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPY SCISSORS 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 1992-03-09 under 510(k) number K915544. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPY SCISSORS?

LAPAROSCOPY SCISSORS is a medical device that received FDA 510(k) clearance on 1992-03-09. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K915544.

When did LAPAROSCOPY SCISSORS receive FDA 510(k) clearance?

LAPAROSCOPY SCISSORS received FDA 510(k) clearance on 1992-03-09, under 510(k) number K915544.

Who is the listed applicant for LAPAROSCOPY SCISSORS?

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 LAPAROSCOPY SCISSORS?

The FDA product code for LAPAROSCOPY SCISSORS is GCJ.

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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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