PARASPA PARAFFIN BATH, PARASPAP MINI, PARASPA ULTRA— 510(k) K001860

Name: FDA 510(k) clearance K001860
Creator: U.S. Food and Drug Administration
Published: 2000-08-10

Substantially Equivalent

Homedics, Inc.

FDA 510(k) clearance K001860 for PARASPA PARAFFIN BATH, PARASPAP MINI, PARASPA ULTRA, Substantially Equivalent on 2000-08-10. Applicant: Homedics, Inc.. Device class: 2.

Clearance details

Applicant: Homedics, Inc.
Product code: Code IMC
Device class: Class 2
Regulation: 21 CFR 890.5110
Advisory panel: Physical Medicine
Date received: 2000-06-19
Decision date: 2000-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Commerce Township, MI, US

Download summary PDF View on FDA.gov ↗

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