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FDA 510(k)

HEALTLH ESSENTIALS PERSONAL MASSAGER

K-Number: K924431 · 1993-10-12

ApplicantConair Corp.
Decision Date1993-10-12
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEALTLH ESSENTIALS PERSONAL 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 1993-10-12 under 510(k) number K924431. 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 HEALTLH ESSENTIALS PERSONAL MASSAGER?

HEALTLH ESSENTIALS PERSONAL MASSAGER is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Conair Corp.. The 510(k) number is K924431.

When did HEALTLH ESSENTIALS PERSONAL MASSAGER receive FDA 510(k) clearance?

HEALTLH ESSENTIALS PERSONAL MASSAGER received FDA 510(k) clearance on 1993-10-12, under 510(k) number K924431.

Who is the listed applicant for HEALTLH ESSENTIALS PERSONAL 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 HEALTLH ESSENTIALS PERSONAL MASSAGER?

The FDA product code for HEALTLH ESSENTIALS PERSONAL 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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