AUTIMO— 510(k) K971001

Substantially Equivalent

Medizintechnik, GmbH

FDA 510(k) clearance K971001 for AUTIMO, Substantially Equivalent on 1997-06-13. Applicant: Medizintechnik, GmbH. Device class: 2.

Clearance details

Applicant: Medizintechnik, GmbH
Product code: Code IXI
Device class: Class 2
Regulation: 21 CFR 892.5710
Advisory panel: Radiology
Date received: 1997-03-19
Decision date: 1997-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, 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.