MULTIX SELECT DR— 510(k) K132934

Substantially Equivalent

Siemens Medi Cal Solutions, Inc.

FDA 510(k) clearance K132934 for MULTIX SELECT DR, Substantially Equivalent on 2014-04-10. Applicant: Siemens Medi Cal Solutions, Inc..

Clearance details

Applicant: Siemens Medi Cal Solutions, Inc.
Product code: Code KPR
Advisory panel: Radiology
Date received: 2013-09-18
Decision date: 2014-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mavern, PA, US

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Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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