SHORTWAVE EPILATOR FOR PERMANENT HAIR REMOVAL— 510(k) K941227

Name: FDA 510(k) clearance K941227
Creator: U.S. Food and Drug Administration
Published: 1994-08-18

Substantially Equivalent

Instantron

FDA 510(k) clearance K941227 for SHORTWAVE EPILATOR FOR PERMANENT HAIR REMOVAL, Substantially Equivalent on 1994-08-18. Applicant: Instantron. Device class: 1.

Clearance details

Applicant: Instantron
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1994-03-08
Decision date: 1994-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Providence, RI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCW

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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

More clearances from Instantron

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K943398 — THE BLENDTONE ROYALE1994-09-16
K943399 — THE SS-991994-09-16
K931062 — THE VP500 EPILATOR1993-07-08
K931063 — THE ELITE EPILATOR1993-07-08
K931064 — THE BLENDTONE EPILATOR1993-07-08

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