DAPELLE HAIR REMOVER— 510(k) K973773

Substantially Equivalent

Wellquest Intl., Inc.

FDA 510(k) clearance K973773 for DAPELLE HAIR REMOVER, Substantially Equivalent on 1997-12-17. Applicant: Wellquest Intl., Inc.. Device class: 1.

Clearance details

Applicant: Wellquest Intl., Inc.
Product code: Code KCX
Device class: Class 1
Regulation: 21 CFR 878.5360
Advisory panel: General, Plastic Surgery
Date received: 1997-10-02
Decision date: 1997-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCX

K973340 — TWEEZER-TYPE EPILATOR1997-12-03
K973174 — SONIQUE HAIR REMOVER1997-10-30
K973179 — FEMINIQUE SONIC HAIR REMOVER1997-10-30
K972695 — FINALLY FREE1997-10-22
K970338 — TWEEZER-TYPE EPILATOR1997-07-01

More clearances from Wellquest Intl., Inc.

K132518 — NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE2014-08-17

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