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FDA 510(k)

WINDMERE WAND MASSAGER

K-Number: K932904 · 1994-02-17

ApplicantWindmere Corp.
Decision Date1994-02-17
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WINDMERE WAND MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Windmere Corp.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K932904. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINDMERE WAND MASSAGER?

WINDMERE WAND MASSAGER is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Windmere Corp.. The 510(k) number is K932904.

When did WINDMERE WAND MASSAGER receive FDA 510(k) clearance?

WINDMERE WAND MASSAGER received FDA 510(k) clearance on 1994-02-17, under 510(k) number K932904.

Who is the listed applicant for WINDMERE WAND MASSAGER?

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 WAND MASSAGER?

The FDA product code for WINDMERE WAND MASSAGER is ISA.

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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.

K980769WINDMERE MODEL DS-2 FOOT BATHK933974WINDMERE MASSAGE MATEK924237WINDMERE PRELUDE IIIK931086WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGERK912659SOUND RELIEFK896245PLAK TRAC POWERED TOOTHBRUSH

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Related Devices (Code: ISA)

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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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