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FDA 510(k)

LAPAROSCOPY INSTRUMENTS

K-Number: K931778 · 1994-04-12

ApplicantBuckman Co., Inc.
Decision Date1994-04-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1994-04-12 under 510(k) number K931778. 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 INSTRUMENTS?

LAPAROSCOPY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Buckman Co., Inc.. The 510(k) number is K931778.

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

LAPAROSCOPY INSTRUMENTS received FDA 510(k) clearance on 1994-04-12, under 510(k) number K931778.

Who is the listed applicant for LAPAROSCOPY INSTRUMENTS?

The FDA 510(k) record lists Buckman Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPY INSTRUMENTS?

The FDA product code for LAPAROSCOPY INSTRUMENTS 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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