FDA 510(k)

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22

K-Number: K942579 · 1994-09-21

Decision Date1994-09-21

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-09-21 under 510(k) number K942579. 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 MODEL NO. GSU-20 AND GSU-22?

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 is a medical device that received FDA 510(k) clearance on 1994-09-21. The listed applicant is Valleylab, Inc.. The 510(k) number is K942579.

When did FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 receive FDA 510(k) clearance?

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 received FDA 510(k) clearance on 1994-09-21, under 510(k) number K942579.

Who is the listed applicant for FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22?

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 MODEL NO. GSU-20 AND GSU-22?

The FDA product code for FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 is GEI.

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Other records listing Valleylab, Inc. as applicant

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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.