FO51/F151 GOLF MASSAGER
K-Number: K914706 · 1991-12-09
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Device Summary
Frequently Asked Questions
What is the FO51/F151 GOLF MASSAGER?
FO51/F151 GOLF 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 K914706.
When did FO51/F151 GOLF MASSAGER receive FDA 510(k) clearance?
FO51/F151 GOLF MASSAGER received FDA 510(k) clearance on 1991-12-09, under 510(k) number K914706.
Who is the listed applicant for FO51/F151 GOLF 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 FO51/F151 GOLF MASSAGER?
The FDA product code for FO51/F151 GOLF 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.
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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