WM10, WM20, WM30 POWER MASSAGER
K-Number: K862041 · 1986-06-17
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Device Summary
Frequently Asked Questions
What is the WM10, WM20, WM30 POWER MASSAGER?
WM10, WM20, WM30 POWER MASSAGER is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Associated Mills, Inc.. The 510(k) number is K862041.
When did WM10, WM20, WM30 POWER MASSAGER receive FDA 510(k) clearance?
WM10, WM20, WM30 POWER MASSAGER received FDA 510(k) clearance on 1986-06-17, under 510(k) number K862041.
Who is the listed applicant for WM10, WM20, WM30 POWER MASSAGER?
The FDA 510(k) record lists Associated Mills, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WM10, WM20, WM30 POWER MASSAGER?
The FDA product code for WM10, WM20, WM30 POWER MASSAGER is ISA.
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 Associated Mills, Inc. 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: ISA)
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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