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FDA 510(k)

CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS

K-Number: K923646 · 1992-12-21

ApplicantCodman & Shurtleff, Inc.
Decision Date1992-12-21
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1992-12-21 under 510(k) number K923646. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS?

CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1992-12-21. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K923646.

When did CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS receive FDA 510(k) clearance?

CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS received FDA 510(k) clearance on 1992-12-21, under 510(k) number K923646.

Who is the listed applicant for CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS?

The FDA product code for CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS is GWG.

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Related Devices (Code: GWG)

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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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