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FDA 510(k)

5MM MICROSCISSORS

K-Number: K913870 · 1991-09-16

ApplicantEndovations
Decision Date1991-09-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

5MM MICROSCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Endovations. It received FDA 510(k) clearance on 1991-09-16 under 510(k) number K913870. 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 5MM MICROSCISSORS?

5MM MICROSCISSORS is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Endovations. The 510(k) number is K913870.

When did 5MM MICROSCISSORS receive FDA 510(k) clearance?

5MM MICROSCISSORS received FDA 510(k) clearance on 1991-09-16, under 510(k) number K913870.

Who is the listed applicant for 5MM MICROSCISSORS?

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

What is the FDA product code for 5MM MICROSCISSORS?

The FDA product code for 5MM MICROSCISSORS is GCJ.

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Other records listing Endovations as applicant

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K955413ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETERK942110INJECT-SNAREK934315ENDOVATIONS(R) .035 PRE-CUT PAPILLATOMEK9138412 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATHK911155OVAL CUP BIOPSY FORCEPK892218ENDO-SPONGE

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Related Devices (Code: 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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