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)

TWEEZER-TYPE EPILATOR

K-Number: K973340 · 1997-12-03

ApplicantMobit, Inc.
Decision Date1997-12-03
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TWEEZER-TYPE EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mobit, Inc.. It received FDA 510(k) clearance on 1997-12-03 under 510(k) number K973340. The device is classified under product code KCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TWEEZER-TYPE EPILATOR?

TWEEZER-TYPE EPILATOR is a medical device that received FDA 510(k) clearance on 1997-12-03. The listed applicant is Mobit, Inc.. The 510(k) number is K973340.

When did TWEEZER-TYPE EPILATOR receive FDA 510(k) clearance?

TWEEZER-TYPE EPILATOR received FDA 510(k) clearance on 1997-12-03, under 510(k) number K973340.

Who is the listed applicant for TWEEZER-TYPE EPILATOR?

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

What is the FDA product code for TWEEZER-TYPE EPILATOR?

The FDA product code for TWEEZER-TYPE EPILATOR is KCX.

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

Related Devices (Code: KCX)

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.

K973773DAPELLE HAIR REMOVERWellquest Intl., Inc.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K973179FEMINIQUE SONIC HAIR REMOVERGlobal TV Concepts, Ltd.K972695FINALLY FREEMehl/Group MarketingK970338TWEEZER-TYPE EPILATORIgia Direct, Inc.K935706EPI 2Universal H.R. System, Inc.

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.

↑