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FDA 510(k)

FAMILY FITNESS SHIATSU MASSAGER

K-Number: K943092 · 1994-09-29

ApplicantConair Corp.
Decision Date1994-09-29
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FAMILY FITNESS SHIATSU MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943092. 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 FAMILY FITNESS SHIATSU MASSAGER?

FAMILY FITNESS SHIATSU MASSAGER is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Conair Corp.. The 510(k) number is K943092.

When did FAMILY FITNESS SHIATSU MASSAGER receive FDA 510(k) clearance?

FAMILY FITNESS SHIATSU MASSAGER received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943092.

Who is the listed applicant for FAMILY FITNESS SHIATSU MASSAGER?

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 FAMILY FITNESS SHIATSU MASSAGER?

The FDA product code for FAMILY FITNESS SHIATSU MASSAGER is ISA.

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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 WRAPK942950BODY FLEX

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Related Devices (Code: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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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