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HAIR REMOVAL SYSTEM

K945192 Class I Traditional
Decision Date
1995-01-12
Sponsor / Applicant
L.P. Systems Corp.

Technical Specification

510(k) Submission ID K945192
Product Code KCW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5350
Decision Date 1995-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HAIR REMOVAL SYSTEM received FDA 510(k) clearance under submission number K945192, sponsored by L.P. Systems Corp.. 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 1995-01-12.

Classification & Regulation

This clearance is catalogued under FDA product code KCW and 21 CFR 878.5350, within the General, Plastic Surgery review panel as a Class I device.