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FDA 510(k)

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP

K-Number: K911243 · 1991-06-19

ApplicantNorthgate Technologies, Inc.
Decision Date1991-06-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP 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 1991-06-19 under 510(k) number K911243. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP?

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP is a medical device that received FDA 510(k) clearance on 1991-06-19. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911243.

When did CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP receive FDA 510(k) clearance?

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP received FDA 510(k) clearance on 1991-06-19, under 510(k) number K911243.

Who is the listed applicant for CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP?

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 CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP?

The FDA product code for CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP is GCJ.

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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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