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FEMINIQUE SONIC HAIR REMOVER

K973179 Class I Traditional
Decision Date
1997-10-30
Sponsor / Applicant
Global TV Concepts, Ltd.

Technical Specification

510(k) Submission ID K973179
Product Code KCX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5360
Decision Date 1997-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FEMINIQUE SONIC HAIR REMOVER received FDA 510(k) clearance under submission number K973179, sponsored by Global TV Concepts, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1997-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code KCX and 21 CFR 878.5360, within the General, Plastic Surgery review panel as a Class I device.