WINDMERE MASSAGE MATE
K-Number: K933974 · 1994-02-02
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Device Summary
Frequently Asked Questions
What is the WINDMERE MASSAGE MATE?
WINDMERE MASSAGE MATE is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Windmere Corp.. The 510(k) number is K933974.
When did WINDMERE MASSAGE MATE receive FDA 510(k) clearance?
WINDMERE MASSAGE MATE received FDA 510(k) clearance on 1994-02-02, under 510(k) number K933974.
Who is the listed applicant for WINDMERE MASSAGE MATE?
The FDA 510(k) record lists Windmere Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WINDMERE MASSAGE MATE?
The FDA product code for WINDMERE MASSAGE MATE 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 Windmere 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.
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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