NEOTONUS MS-101 MAGNETIC MUSCLE STIMULATOR SYSTEM— 510(k) K973929

Name: FDA 510(k) clearance K973929
Creator: U.S. Food and Drug Administration
Published: 1998-05-21

Substantially Equivalent

Neotonus, Inc.

FDA 510(k) clearance K973929 for NEOTONUS MS-101 MAGNETIC MUSCLE STIMULATOR SYSTEM, Substantially Equivalent on 1998-05-21. Applicant: Neotonus, Inc.. Device class: 2.

Clearance details

Applicant: Neotonus, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1997-10-15
Decision date: 1998-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

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