REMINGTON PARAFFIN SPA, MODELS HS-200. PFS-600— 510(k) K013328

Name: FDA 510(k) clearance K013328
Creator: U.S. Food and Drug Administration
Published: 2001-12-03

Substantially Equivalent

Remington Products Company, LLC

FDA 510(k) clearance K013328 for REMINGTON PARAFFIN SPA, MODELS HS-200. PFS-600, Substantially Equivalent on 2001-12-03. Applicant: Remington Products Company, LLC. Device class: 2.

Clearance details

Applicant: Remington Products Company, LLC
Product code: Code IMC
Device class: Class 2
Regulation: 21 CFR 890.5110
Advisory panel: Physical Medicine
Date received: 2001-10-05
Decision date: 2001-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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