TWEEZER-TYPE EPILATOR— 510(k) K970338

Substantially Equivalent

Igia Direct, Inc.

FDA 510(k) clearance K970338 for TWEEZER-TYPE EPILATOR, Substantially Equivalent on 1997-07-01. Applicant: Igia Direct, Inc.. Device class: 1.

Clearance details

Applicant: Igia Direct, Inc.
Product code: Code KCX
Device class: Class 1
Regulation: 21 CFR 878.5360
Advisory panel: General, Plastic Surgery
Date received: 1997-01-29
Decision date: 1997-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westford, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCX

K973773 — DAPELLE HAIR REMOVER1997-12-17
K973340 — TWEEZER-TYPE EPILATOR1997-12-03
K973174 — SONIQUE HAIR REMOVER1997-10-30
K973179 — FEMINIQUE SONIC HAIR REMOVER1997-10-30
K972695 — FINALLY FREE1997-10-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.