LINDSTROM CORDLESS EPILATOR— 510(k) K883429

Name: FDA 510(k) clearance K883429
Creator: U.S. Food and Drug Administration
Published: 1988-09-28

Substantially Equivalent

A Place of Health & Beauty

FDA 510(k) clearance K883429 for LINDSTROM CORDLESS EPILATOR, Substantially Equivalent on 1988-09-28. Applicant: A Place of Health & Beauty. Device class: 1.

Clearance details

Applicant: A Place of Health & Beauty
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1988-08-15
Decision date: 1988-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Costa Mesa, CA, US

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K943396 — THE ELITE SPECTRUM1994-09-16

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