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FDA 510(k)

ENDOSCOPE AND ACCESSORIES

K-Number: K905117 · 1991-04-25

ApplicantNorthgate Technologies, Inc.
Decision Date1991-04-25
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1991-04-25 under 510(k) number K905117. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPE AND ACCESSORIES?

ENDOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K905117.

When did ENDOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

ENDOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1991-04-25, under 510(k) number K905117.

Who is the listed applicant for ENDOSCOPE AND ACCESSORIES?

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

What is the FDA product code for ENDOSCOPE AND ACCESSORIES?

The FDA product code for ENDOSCOPE AND ACCESSORIES is GCI.

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Related Devices (Code: GCI)

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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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