HANDMASTER NMS1— 510(k) K982482

Name: FDA 510(k) clearance K982482
Creator: U.S. Food and Drug Administration
Published: 1998-09-30

Substantially Equivalent

N.E.S.S. Nuromuscular Electrical Stimulation Syst

FDA 510(k) clearance K982482 for HANDMASTER NMS1, Substantially Equivalent on 1998-09-30. Applicant: N.E.S.S. Nuromuscular Electrical Stimulation Syst. Device class: 2.

Clearance details

Applicant: N.E.S.S. Nuromuscular Electrical Stimulation Syst
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1998-07-16
Decision date: 1998-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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