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FDA 510(k)

VALLEYLAB FORCE FX

K-Number: K944602 · 1995-06-05

ApplicantValleylab, Inc.
Decision Date1995-06-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB FORCE FX is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1995-06-05 under 510(k) number K944602. 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 VALLEYLAB FORCE FX?

VALLEYLAB FORCE FX is a medical device that received FDA 510(k) clearance on 1995-06-05. The listed applicant is Valleylab, Inc.. The 510(k) number is K944602.

When did VALLEYLAB FORCE FX receive FDA 510(k) clearance?

VALLEYLAB FORCE FX received FDA 510(k) clearance on 1995-06-05, under 510(k) number K944602.

Who is the listed applicant for VALLEYLAB FORCE FX?

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 VALLEYLAB FORCE FX?

The FDA product code for VALLEYLAB FORCE FX is GEI.

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Other records listing Valleylab, Inc. as applicant

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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Related Devices (Code: 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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