FDA 510(k)

LECTROVAC, VALLEYLAB MODELS

K-Number: K791752 · 1979-10-04

Decision Date1979-10-04

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LECTROVAC, VALLEYLAB MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791752. 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 LECTROVAC, VALLEYLAB MODELS?

LECTROVAC, VALLEYLAB MODELS is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Valleylab, Inc.. The 510(k) number is K791752.

When did LECTROVAC, VALLEYLAB MODELS receive FDA 510(k) clearance?

LECTROVAC, VALLEYLAB MODELS received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791752.

Who is the listed applicant for LECTROVAC, VALLEYLAB MODELS?

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 LECTROVAC, VALLEYLAB MODELS?

The FDA product code for LECTROVAC, VALLEYLAB MODELS 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.