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FDA 510(k)

LAPAROSCOPIC RINSING CONTAINER

K-Number: K911488 · 1991-06-06

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-06-06
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC RINSING CONTAINER 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 1991-06-06 under 510(k) number K911488. 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 RINSING CONTAINER?

LAPAROSCOPIC RINSING CONTAINER is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911488.

When did LAPAROSCOPIC RINSING CONTAINER receive FDA 510(k) clearance?

LAPAROSCOPIC RINSING CONTAINER received FDA 510(k) clearance on 1991-06-06, under 510(k) number K911488.

Who is the listed applicant for LAPAROSCOPIC RINSING CONTAINER?

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 RINSING CONTAINER?

The FDA product code for LAPAROSCOPIC RINSING CONTAINER is GCJ.

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Related Devices (Code: 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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