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FDA 510(k)

BODY FLEX

K-Number: K942950 · 1994-07-26

ApplicantConair Corp.
Decision Date1994-07-26
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

BODY FLEX is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-07-26 under 510(k) number K942950. 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 FLEX?

BODY FLEX is a medical device that received FDA 510(k) clearance on 1994-07-26. The listed applicant is Conair Corp.. The 510(k) number is K942950.

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

BODY FLEX received FDA 510(k) clearance on 1994-07-26, under 510(k) number K942950.

Who is the listed applicant for BODY FLEX?

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 FLEX?

The FDA product code for BODY FLEX is ISA.

Other records listing Conair Corp. as applicant

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.

K950441CONAIR FAMILY FITNESS BODY ENERGYK950410CONAIR BODY AND SOLEK944637FAMILY FITNESS SHIATSU MASSAGERK943730SQUEEZE PLAYK924970FEMININE HEAT WRAPK943092FAMILY FITNESS SHIATSU MASSAGER

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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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