FDA 510(k)

ELECTRONIC CELL ENERGIZER

K-Number: K834293 · 1984-01-13

Decision Date1984-01-13

Product CodeLBG

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ELECTRONIC CELL ENERGIZER is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Energy, Inc.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K834293. The device is classified under product code LBG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC CELL ENERGIZER?

ELECTRONIC CELL ENERGIZER is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Electronic Energy, Inc.. The 510(k) number is K834293.

When did ELECTRONIC CELL ENERGIZER receive FDA 510(k) clearance?

ELECTRONIC CELL ENERGIZER received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834293.

Who is the listed applicant for ELECTRONIC CELL ENERGIZER?

The FDA 510(k) record lists Electronic Energy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC CELL ENERGIZER?

The FDA product code for ELECTRONIC CELL ENERGIZER is LBG.

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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.