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FDA 510(k)

FORCE 10, 20, 30, AND 40

K-Number: K905605 · 1991-03-14

ApplicantValleylab, Inc.
Decision Date1991-03-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCE 10, 20, 30, AND 40 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1991-03-14 under 510(k) number K905605. 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 10, 20, 30, AND 40?

FORCE 10, 20, 30, AND 40 is a medical device that received FDA 510(k) clearance on 1991-03-14. The listed applicant is Valleylab, Inc.. The 510(k) number is K905605.

When did FORCE 10, 20, 30, AND 40 receive FDA 510(k) clearance?

FORCE 10, 20, 30, AND 40 received FDA 510(k) clearance on 1991-03-14, under 510(k) number K905605.

Who is the listed applicant for FORCE 10, 20, 30, AND 40?

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 10, 20, 30, AND 40?

The FDA product code for FORCE 10, 20, 30, AND 40 is GEI.

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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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