NEUROTECH MEDISTIM PLUS, TYPE 291— 510(k) K014019

Name: FDA 510(k) clearance K014019
Creator: U.S. Food and Drug Administration
Published: 2002-07-11

Substantially Equivalent

Bio-Medical Research, Ltd.

FDA 510(k) clearance K014019 for NEUROTECH MEDISTIM PLUS, TYPE 291, Substantially Equivalent on 2002-07-11. Applicant: Bio-Medical Research, Ltd.. Device class: 2.

Clearance details

Applicant: Bio-Medical Research, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2001-12-06
Decision date: 2002-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

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