KOORDINAT ANGIO— 510(k) K781992

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K781992 for KOORDINAT ANGIO, Substantially Equivalent on 1978-12-07. Applicant: Siemens Corp.. Device class: 2.

Clearance details

Applicant: Siemens Corp.
Product code: Code KXJ
Device class: Class 2
Regulation: 21 CFR 892.1980
Advisory panel: Radiology
Date received: 1978-11-24
Decision date: 1978-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.