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FDA 510(k)

MULTI-REACH II WAND MASSAGER

K-Number: K914344 · 1991-10-24

ApplicantConair Corp.
Decision Date1991-10-24
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTI-REACH II WAND 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 1991-10-24 under 510(k) number K914344. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-REACH II WAND MASSAGER?

MULTI-REACH II WAND MASSAGER is a medical device that received FDA 510(k) clearance on 1991-10-24. The listed applicant is Conair Corp.. The 510(k) number is K914344.

When did MULTI-REACH II WAND MASSAGER receive FDA 510(k) clearance?

MULTI-REACH II WAND MASSAGER received FDA 510(k) clearance on 1991-10-24, under 510(k) number K914344.

Who is the listed applicant for MULTI-REACH II WAND 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 MULTI-REACH II WAND MASSAGER?

The FDA product code for MULTI-REACH II WAND MASSAGER is IRO.

Related Clinical Trials

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.

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.

View all 29 devices →

Related Devices (Code: IRO)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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