REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER— 510(k) K895409

Name: FDA 510(k) clearance K895409
Creator: U.S. Food and Drug Administration
Published: 1989-10-20

Substantially Equivalent

Remington Products Company, LLC

FDA 510(k) clearance K895409 for REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER, Substantially Equivalent on 1989-10-20. Applicant: Remington Products Company, LLC. Device class: 2.

Clearance details

Applicant: Remington Products Company, LLC
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 1989-09-06
Decision date: 1989-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bridgeport, CT, US

Download summary PDF View on FDA.gov ↗

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