CMAP PRO— 510(k) K113074

Substantially Equivalent

Medical Technologies, Inc.

FDA 510(k) clearance K113074 for CMAP PRO, Substantially Equivalent on 2012-02-02. Applicant: Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Medical Technologies, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2011-10-17
Decision date: 2012-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.