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FDA 510(k)

THE VARIABLE LOAD KENETIC ENERGIZER

K-Number: K792642 · 1980-01-28

ApplicantW.F. Pogue
Decision Date1980-01-28
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE VARIABLE LOAD KENETIC ENERGIZER is the device name listed in this FDA 510(k) record. The listed applicant is W.F. Pogue. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K792642. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VARIABLE LOAD KENETIC ENERGIZER?

THE VARIABLE LOAD KENETIC ENERGIZER is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is W.F. Pogue. The 510(k) number is K792642.

When did THE VARIABLE LOAD KENETIC ENERGIZER receive FDA 510(k) clearance?

THE VARIABLE LOAD KENETIC ENERGIZER received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792642.

Who is the listed applicant for THE VARIABLE LOAD KENETIC ENERGIZER?

The FDA 510(k) record lists W.F. Pogue as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE VARIABLE LOAD KENETIC ENERGIZER?

The FDA product code for THE VARIABLE LOAD KENETIC ENERGIZER is ION.

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Related Devices (Code: ION)

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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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.

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