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FDA 510(k)

BODY RELAXER

K-Number: K926339 · 1994-03-04

ApplicantConair Corp.
Decision Date1994-03-04
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BODY RELAXER is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-03-04 under 510(k) number K926339. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODY RELAXER?

BODY RELAXER is a medical device that received FDA 510(k) clearance on 1994-03-04. The listed applicant is Conair Corp.. The 510(k) number is K926339.

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

BODY RELAXER received FDA 510(k) clearance on 1994-03-04, under 510(k) number K926339.

Who is the listed applicant for BODY RELAXER?

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 RELAXER?

The FDA product code for BODY RELAXER is ISA.

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Other records listing Conair Corp. as applicant

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Related Devices (Code: 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.

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