NEUROTECH-4 PROGRAM NEUROMUSCULAR STIMULATOR 281— 510(k) K860314

Name: FDA 510(k) clearance K860314
Creator: U.S. Food and Drug Administration
Published: 1986-06-17

Substantially Equivalent

Neurotech, Inc.

FDA 510(k) clearance K860314 for NEUROTECH-4 PROGRAM NEUROMUSCULAR STIMULATOR 281, Substantially Equivalent on 1986-06-17. Applicant: Neurotech, Inc.. Device class: 2.

Clearance details

Applicant: Neurotech, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1986-01-28
Decision date: 1986-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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