Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER

K-Number: K931086 · 1993-09-30

ApplicantWindmere Corp.
Decision Date1993-09-30
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WINDMERE VIBRA TOUCH PERSONAL BODY 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 1993-09-30 under 510(k) number K931086. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER?

WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER is a medical device that received FDA 510(k) clearance on 1993-09-30. The listed applicant is Windmere Corp.. The 510(k) number is K931086.

When did WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER receive FDA 510(k) clearance?

WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER received FDA 510(k) clearance on 1993-09-30, under 510(k) number K931086.

Who is the listed applicant for WINDMERE VIBRA TOUCH PERSONAL BODY 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 VIBRA TOUCH PERSONAL BODY MASSAGER?

The FDA product code for WINDMERE VIBRA TOUCH PERSONAL BODY 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 BATHK932904WINDMERE WAND MASSAGERK933974WINDMERE MASSAGE MATEK924237WINDMERE PRELUDE IIIK912659SOUND RELIEFK896245PLAK TRAC POWERED TOOTHBRUSH

View all 7 devices →

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.

K955160COMFORT, MUSCLE, CORDLESS MASSAGER, BATTERY POWERED OPERATED MASSAGEREverapex Design & Marketing Corp.K955250QI GONG MASSAGEREast Health Development Group, Inc.K954203MASSAGER THERAPUTIC, ELECTRICCisco Sales Corp.K952916SHIATSU MASTER MASSAGER CUSHIONKinsei Shiatsu, Inc.K951414CHAMPION PHYSIOACOUSTICC RECLINER-TRANSPORTER CHAIRChampion Mfg. Corp.K950441CONAIR FAMILY FITNESS BODY ENERGYConair Corp.

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.

↑