FDA 510(k)

SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE

K-Number: K951905 · 1995-07-11

Decision Date1995-07-11

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE is the device name listed in this FDA 510(k) record. The listed applicant is H.S. Intl. Co., Inc.. It received FDA 510(k) clearance on 1995-07-11 under 510(k) number K951905. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE?

SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is H.S. Intl. Co., Inc.. The 510(k) number is K951905.

When did SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE receive FDA 510(k) clearance?

SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE received FDA 510(k) clearance on 1995-07-11, under 510(k) number K951905.

Who is the listed applicant for SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE?

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

What is the FDA product code for SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE?

The FDA product code for SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE is GEI.

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Other records listing H.S. Intl. Co., Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.