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FDA 510(k)

CODMAN GAAB NEUROENDOSCOPE

K-Number: K923555 · 1993-03-23

ApplicantCodman & Shurtleff, Inc.
Decision Date1993-03-23
Product CodeGWB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CODMAN GAAB NEUROENDOSCOPE 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 1993-03-23 under 510(k) number K923555. The device is classified under product code GWB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN GAAB NEUROENDOSCOPE?

CODMAN GAAB NEUROENDOSCOPE is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K923555.

When did CODMAN GAAB NEUROENDOSCOPE receive FDA 510(k) clearance?

CODMAN GAAB NEUROENDOSCOPE received FDA 510(k) clearance on 1993-03-23, under 510(k) number K923555.

Who is the listed applicant for CODMAN GAAB NEUROENDOSCOPE?

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 GAAB NEUROENDOSCOPE?

The FDA product code for CODMAN GAAB NEUROENDOSCOPE is GWB.

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Related Devices (Code: GWB)

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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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