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FDA 510(k)

LAPAROSCOPIC SUCTION/IRRIGATION CANNULA

K-Number: K911486 · 1991-04-25

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-04-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC SUCTION/IRRIGATION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1991-04-25 under 510(k) number K911486. 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 LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?

LAPAROSCOPIC SUCTION/IRRIGATION CANNULA is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911486.

When did LAPAROSCOPIC SUCTION/IRRIGATION CANNULA receive FDA 510(k) clearance?

LAPAROSCOPIC SUCTION/IRRIGATION CANNULA received FDA 510(k) clearance on 1991-04-25, under 510(k) number K911486.

Who is the listed applicant for LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?

The FDA product code for LAPAROSCOPIC SUCTION/IRRIGATION CANNULA is GCJ.

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Related Devices (Code: GCJ)

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.

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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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