SIDOS U.— 510(k) K803124

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K803124 for SIDOS U., Substantially Equivalent on 1981-01-22. Applicant: Siemens Corp.. Device class: 2.

Clearance details

Applicant: Siemens Corp.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1980-12-11
Decision date: 1981-01-22
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.