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FDA 510(k)

SCISSORS,GRASPERS,FORCEPS

K-Number: K911754 · 1991-07-17

ApplicantAmerican Cynamid Co.
Decision Date1991-07-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SCISSORS,GRASPERS,FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is American Cynamid Co.. It received FDA 510(k) clearance on 1991-07-17 under 510(k) number K911754. 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 SCISSORS,GRASPERS,FORCEPS?

SCISSORS,GRASPERS,FORCEPS is a medical device that received FDA 510(k) clearance on 1991-07-17. The listed applicant is American Cynamid Co.. The 510(k) number is K911754.

When did SCISSORS,GRASPERS,FORCEPS receive FDA 510(k) clearance?

SCISSORS,GRASPERS,FORCEPS received FDA 510(k) clearance on 1991-07-17, under 510(k) number K911754.

Who is the listed applicant for SCISSORS,GRASPERS,FORCEPS?

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

What is the FDA product code for SCISSORS,GRASPERS,FORCEPS?

The FDA product code for SCISSORS,GRASPERS,FORCEPS is GCJ.

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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.

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