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FDA 510(k)

LAPAROSCOPIC LASER FIBER DIVERTER

K-Number: K912502 · 1991-07-25

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-07-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC LASER FIBER DIVERTER 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 1991-07-25 under 510(k) number K912502. 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 LASER FIBER DIVERTER?

LAPAROSCOPIC LASER FIBER DIVERTER is a medical device that received FDA 510(k) clearance on 1991-07-25. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K912502.

When did LAPAROSCOPIC LASER FIBER DIVERTER receive FDA 510(k) clearance?

LAPAROSCOPIC LASER FIBER DIVERTER received FDA 510(k) clearance on 1991-07-25, under 510(k) number K912502.

Who is the listed applicant for LAPAROSCOPIC LASER FIBER DIVERTER?

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 LASER FIBER DIVERTER?

The FDA product code for LAPAROSCOPIC LASER FIBER DIVERTER 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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