EPILATOR, MULTIPLE NEEDLE-MODEL EM-20— 510(k) K811501

Name: FDA 510(k) clearance K811501
Creator: U.S. Food and Drug Administration
Published: 1981-07-10

Substantially Equivalent

Rcx-Western, Inc.

FDA 510(k) clearance K811501 for EPILATOR, MULTIPLE NEEDLE-MODEL EM-20, Substantially Equivalent on 1981-07-10. Applicant: Rcx-Western, Inc.. Device class: 1.

Clearance details

Applicant: Rcx-Western, Inc.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1981-05-27
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K943396 — THE ELITE SPECTRUM1994-09-16

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K811502 — STIMULATOR, FACIAL-MODELS SF-100 & 2001981-07-24
K811503 — EPILATOR, BLEND-MODEL EB-200 & ET-11981-07-10

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