FDA 510(k)

MODEL FORCE 2 ELECTROSURGICAL GENERATOR

K-Number: K844403 · 1985-02-20

Decision Date1985-02-20

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODEL FORCE 2 ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1985-02-20 under 510(k) number K844403. 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 MODEL FORCE 2 ELECTROSURGICAL GENERATOR?

MODEL FORCE 2 ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1985-02-20. The listed applicant is Valleylab, Inc.. The 510(k) number is K844403.

When did MODEL FORCE 2 ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

MODEL FORCE 2 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1985-02-20, under 510(k) number K844403.

Who is the listed applicant for MODEL FORCE 2 ELECTROSURGICAL GENERATOR?

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 MODEL FORCE 2 ELECTROSURGICAL GENERATOR?

The FDA product code for MODEL FORCE 2 ELECTROSURGICAL GENERATOR is GEI.

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Other records listing Valleylab, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.