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)

VIBRATOUCH II CORDLESS WAND MASSAGER

K-Number: K912383 · 1991-10-07

ApplicantConair Corp.
Decision Date1991-10-07
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VIBRATOUCH II CORDLESS WAND MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1991-10-07 under 510(k) number K912383. 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 VIBRATOUCH II CORDLESS WAND MASSAGER?

VIBRATOUCH II CORDLESS WAND MASSAGER is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is Conair Corp.. The 510(k) number is K912383.

When did VIBRATOUCH II CORDLESS WAND MASSAGER receive FDA 510(k) clearance?

VIBRATOUCH II CORDLESS WAND MASSAGER received FDA 510(k) clearance on 1991-10-07, under 510(k) number K912383.

Who is the listed applicant for VIBRATOUCH II CORDLESS WAND MASSAGER?

The FDA 510(k) record lists Conair Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIBRATOUCH II CORDLESS WAND MASSAGER?

The FDA product code for VIBRATOUCH II CORDLESS WAND 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.

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 Conair 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.

K950441CONAIR FAMILY FITNESS BODY ENERGYK950410CONAIR BODY AND SOLEK944637FAMILY FITNESS SHIATSU MASSAGERK943730SQUEEZE PLAYK924970FEMININE HEAT WRAPK943092FAMILY FITNESS SHIATSU MASSAGER

View all 29 devices →

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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.

↑