FDA 510(k)

VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET

K-Number: K926481 · 1994-02-12

Decision Date1994-02-12

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-02-12 under 510(k) number K926481. 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 MODEL E252OH, FORCE GSU(TM) HANDSET?

VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET is a medical device that received FDA 510(k) clearance on 1994-02-12. The listed applicant is Valleylab, Inc.. The 510(k) number is K926481.

When did VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET receive FDA 510(k) clearance?

VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET received FDA 510(k) clearance on 1994-02-12, under 510(k) number K926481.

Who is the listed applicant for VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET?

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 MODEL E252OH, FORCE GSU(TM) HANDSET?

The FDA product code for VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET 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.