HIGH FREQUENCY NEEDLE-TYPE EPILATOR— 510(k) K864291

Name: FDA 510(k) clearance K864291
Creator: U.S. Food and Drug Administration
Published: 1986-12-24

Substantially Equivalent

Multi-Channel Epilator

FDA 510(k) clearance K864291 for HIGH FREQUENCY NEEDLE-TYPE EPILATOR, Substantially Equivalent on 1986-12-24. Applicant: Multi-Channel Epilator. Device class: 1.

Clearance details

Applicant: Multi-Channel Epilator
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1986-10-31
Decision date: 1986-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sun Valley, CA, US

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K954031 — COMPU-BLEND EPILATOR1996-01-05
K952611 — STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION1995-10-18
K943928 — APILUS ELECTROPIL1995-01-12
K945192 — HAIR REMOVAL SYSTEM1995-01-12
K943396 — THE ELITE SPECTRUM1994-09-16

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