MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300— 510(k) K030998

Name: FDA 510(k) clearance K030998
Creator: U.S. Food and Drug Administration
Published: 2003-10-10

Substantially Equivalent

Healthonics, Inc.

FDA 510(k) clearance K030998 for MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300, Substantially Equivalent on 2003-10-10. Applicant: Healthonics, Inc.. Device class: 2.

Clearance details

Applicant: Healthonics, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2003-03-31
Decision date: 2003-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Ellenton, SC, US

Download summary PDF View on FDA.gov ↗

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