HANDMASTER NMS1— 510(k) K952273

Name: FDA 510(k) clearance K952273
Creator: U.S. Food and Drug Administration
Published: 1996-05-23

Substantially Equivalent

Neuromusclar Electrical Stimulation Systems, Ltd.

FDA 510(k) clearance K952273 for HANDMASTER NMS1, Substantially Equivalent on 1996-05-23. Applicant: Neuromusclar Electrical Stimulation Systems, Ltd.. Device class: 2.

Clearance details

Applicant: Neuromusclar Electrical Stimulation Systems, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1995-05-15
Decision date: 1996-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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