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FDA 510(k)

REVISED BATTERY CHARGER

K-Number: K790689 · 1979-05-29

ApplicantVickers America Medical Corp.
Decision Date1979-05-29
Product CodeFPL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REVISED BATTERY CHARGER is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1979-05-29 under 510(k) number K790689. The device is classified under product code FPL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVISED BATTERY CHARGER?

REVISED BATTERY CHARGER is a medical device that received FDA 510(k) clearance on 1979-05-29. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K790689.

When did REVISED BATTERY CHARGER receive FDA 510(k) clearance?

REVISED BATTERY CHARGER received FDA 510(k) clearance on 1979-05-29, under 510(k) number K790689.

Who is the listed applicant for REVISED BATTERY CHARGER?

The FDA 510(k) record lists Vickers America Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REVISED BATTERY CHARGER?

The FDA product code for REVISED BATTERY CHARGER is FPL.

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Other records listing Vickers America Medical Corp. 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.

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