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FDA 510(k)

CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)

K-Number: K920979 · 1993-03-23

ApplicantCodman & Shurtleff, Inc.
Decision Date1993-03-23
Product CodeGCQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340) 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 K920979. The device is classified under product code GCQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)?

CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340) 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 K920979.

When did CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340) receive FDA 510(k) clearance?

CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340) received FDA 510(k) clearance on 1993-03-23, under 510(k) number K920979.

Who is the listed applicant for CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)?

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 STEERABLE ENDOSCOPE (CAT.# 83-1340)?

The FDA product code for CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340) is GCQ.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: GCQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K900894MEDILASE SERIES 2100 ENDOSCOPEMedical Laser, Inc.K871978CODMAN FLEXIBLE ENDOSCOPECodman & Shurtleff, Inc.K864960TV-ENDOSCOPE, UPPER & LOWER GASTROINTESTINAL APPL.Cooper Lasersonics, Inc.K860771VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPEVan-Tec, Inc.

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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