F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR
K-Number: K931639 · 1994-03-28
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Device Summary
Frequently Asked Questions
What is the F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR?
F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Fairform Mfg., Co., Ltd.. The 510(k) number is K931639.
When did F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR receive FDA 510(k) clearance?
F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR received FDA 510(k) clearance on 1994-03-28, under 510(k) number K931639.
Who is the listed applicant for F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR?
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 F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR?
The FDA product code for F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR 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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