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FDA 510(k)

FO69 FANCY MASSAGER

K-Number: K914704 · 1991-12-09

Decision Date1991-12-09
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FO69 FANCY MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Fairform Mfg., Co., Ltd.. It received FDA 510(k) clearance on 1991-12-09 under 510(k) number K914704. 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 FO69 FANCY MASSAGER?

FO69 FANCY MASSAGER is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Fairform Mfg., Co., Ltd.. The 510(k) number is K914704.

When did FO69 FANCY MASSAGER receive FDA 510(k) clearance?

FO69 FANCY MASSAGER received FDA 510(k) clearance on 1991-12-09, under 510(k) number K914704.

Who is the listed applicant for FO69 FANCY MASSAGER?

The FDA 510(k) record lists Fairform Mfg., Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FO69 FANCY MASSAGER?

The FDA product code for FO69 FANCY 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 Fairform Mfg., Co., Ltd. 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 13 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

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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