MODIFICATION TO:BREVIO NERVE CONDUCTION TEST INSTRUMENT— 510(k) K012069

Name: FDA 510(k) clearance K012069
Creator: U.S. Food and Drug Administration
Published: 2001-08-01

Substantially Equivalent

Neurotron Medical, Inc.

FDA 510(k) clearance K012069 for MODIFICATION TO:BREVIO NERVE CONDUCTION TEST INSTRUMENT, Substantially Equivalent on 2001-08-01. Applicant: Neurotron Medical, Inc.. Device class: 2.

Clearance details

Applicant: Neurotron Medical, Inc.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 2001-07-02
Decision date: 2001-08-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Rockville, MD, US

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