EXOMIO, MODEL 1.1— 510(k) K022219

Substantially Equivalent

Medcom GmbH

FDA 510(k) clearance K022219 for EXOMIO, MODEL 1.1, Substantially Equivalent on 2002-10-07. Applicant: Medcom GmbH. Device class: 2.

Clearance details

Applicant: Medcom GmbH
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 2002-07-09
Decision date: 2002-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Darmstadt, Hessen, DE

Download summary PDF View on FDA.gov ↗

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