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EPILATION NEEDLE

K894771 Class I Traditional
Decision Date
1989-08-21
Sponsor / Applicant
Precision Electrolysis Needles, Inc.

Technical Specification

510(k) Submission ID K894771
Product Code KCW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5350
Decision Date 1989-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EPILATION NEEDLE received FDA 510(k) clearance under submission number K894771, sponsored by Precision Electrolysis Needles, Inc.. 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 1989-08-21.

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.