NEOTONUS MODEL 1000 MUSCLE STIMULATOR SYSTEM— 510(k) K973096

Substantially Equivalent

Neotonus, Inc.

FDA 510(k) clearance K973096 for NEOTONUS MODEL 1000 MUSCLE STIMULATOR SYSTEM, Substantially Equivalent on 1998-06-12. Applicant: Neotonus, Inc..

Clearance details

Applicant: Neotonus, Inc.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 1997-08-19
Decision date: 1998-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

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