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FDA 510(k)

FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION

K-Number: K922090 · 1992-08-04

ApplicantValleylab, Inc.
Decision Date1992-08-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1992-08-04 under 510(k) number K922090. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION?

FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION is a medical device that received FDA 510(k) clearance on 1992-08-04. The listed applicant is Valleylab, Inc.. The 510(k) number is K922090.

When did FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION receive FDA 510(k) clearance?

FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION received FDA 510(k) clearance on 1992-08-04, under 510(k) number K922090.

Who is the listed applicant for FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION?

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

What is the FDA product code for FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION?

The FDA product code for FORCE GSU SYSTEM W/ LAPAROSCOPIC OPTION is GEI.

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Related Devices (Code: GEI)

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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