EPILATOR, EASE-MULTI-MODE— 510(k) K781147

Name: FDA 510(k) clearance K781147
Creator: U.S. Food and Drug Administration
Published: 1978-10-10

Substantially Equivalent

Greenleaf-Carter Enterprises, Inc.

FDA 510(k) clearance K781147 for EPILATOR, EASE-MULTI-MODE, Substantially Equivalent on 1978-10-10. Applicant: Greenleaf-Carter Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Greenleaf-Carter Enterprises, Inc.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1978-07-10
Decision date: 1978-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCW

view all

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.