FDA 510(k)

BODY RECHARGER

K-Number: K940369 · 1994-04-21

Decision Date1994-04-21

Product CodeISA

Advisory CommitteePM

DecisionSubstantially Equivalent for Some Indications

Device Summary

BODY RECHARGER is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-04-21 under 510(k) number K940369. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BODY RECHARGER?

BODY RECHARGER is a medical device that received FDA 510(k) clearance on 1994-04-21. The listed applicant is Conair Corp.. The 510(k) number is K940369.

When did BODY RECHARGER receive FDA 510(k) clearance?

BODY RECHARGER received FDA 510(k) clearance on 1994-04-21, under 510(k) number K940369.

Who is the listed applicant for BODY RECHARGER?

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

What is the FDA product code for BODY RECHARGER?

The FDA product code for BODY RECHARGER is ISA.

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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.