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Scissors, Graspers, Forceps

by American Cynamid Co.

510(k) K911754

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK911754 Date17 Jul 1991ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
GCJ
Device Class
Class II
Regulation
21 CFR Part 876.1500
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 21 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

Scissors, Grasps, Forceps is a device type comprising surgical instruments used for cutting, grasping, and manipulating tissue during procedures. It is substantially equivalent to a predicate device as determined by FDA 510(k) clearance.

The device was cleared via the traditional 510(k) pathway under product code GCJ, with decision date July 17, 1991, and K number K911754. It was manufactured by American Cynamid Co. and reviewed by the Gastroenterology and Urology advisory committees.

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Questions

AI-generated answers, 21 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the Scissors, Grasps, Forceps device used for?

    The Scissors, Grasps, Forceps device comprises surgical instruments used for cutting, grasping, and manipulating tissue during procedures, as stated in the device description.

  • How was the Scissors, Grasps, Forceps device cleared for market?

    The device was cleared via the traditional 510(k) pathway under product code GCJ, with decision date July 17, 1991, and K number K911754, as determined by FDA 510(k) clearance.

  • Who manufactured the Scissors, Grasps, Forceps device and where was it made?

    The device was manufactured by American Cynamid Co., located at One Casper St., Danbury, CT 06810, US, as specified in the device data.