FDA 510(k)

MODEL FORCE 4B ELECTROSURGICAL GENERATOR

K-Number: K864675 · 1987-01-08

Decision Date1987-01-08

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODEL FORCE 4B 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 1987-01-08 under 510(k) number K864675. 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 4B ELECTROSURGICAL GENERATOR?

MODEL FORCE 4B ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1987-01-08. The listed applicant is Valleylab, Inc.. The 510(k) number is K864675.

When did MODEL FORCE 4B ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

MODEL FORCE 4B ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1987-01-08, under 510(k) number K864675.

Who is the listed applicant for MODEL FORCE 4B 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 4B ELECTROSURGICAL GENERATOR?

The FDA product code for MODEL FORCE 4B ELECTROSURGICAL GENERATOR 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.