SIEMENS ANGIOTRON— 510(k) K811587

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K811587 for SIEMENS ANGIOTRON, Substantially Equivalent on 1981-07-10. Applicant: Siemens Corp.. Device class: 1.

Clearance details

Applicant: Siemens Corp.
Product code: Code IXO
Device class: Class 1
Regulation: 21 CFR 892.1970
Advisory panel: Radiology
Date received: 1981-06-05
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXO

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K791959 — POST EXTRA SYSTOLIC POSTENTLATOR1980-01-09

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