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FDA 510(k)

MEDICAM LAPAROSCOPY ENDOSCOPES

K-Number: K912933 · 1991-10-15

ApplicantKirschner Medical Corp.
Decision Date1991-10-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDICAM LAPAROSCOPY ENDOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1991-10-15 under 510(k) number K912933. 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 MEDICAM LAPAROSCOPY ENDOSCOPES?

MEDICAM LAPAROSCOPY ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1991-10-15. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K912933.

When did MEDICAM LAPAROSCOPY ENDOSCOPES receive FDA 510(k) clearance?

MEDICAM LAPAROSCOPY ENDOSCOPES received FDA 510(k) clearance on 1991-10-15, under 510(k) number K912933.

Who is the listed applicant for MEDICAM LAPAROSCOPY ENDOSCOPES?

The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAM LAPAROSCOPY ENDOSCOPES?

The FDA product code for MEDICAM LAPAROSCOPY ENDOSCOPES is GCJ.

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Other records listing Kirschner Medical Corp. as applicant

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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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