SIRECUST 311S— 510(k) K800593

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K800593 for SIRECUST 311S, Substantially Equivalent on 1980-04-02. Applicant: Siemens Corp..

Clearance details

Applicant: Siemens Corp.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1980-03-17
Decision date: 1980-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.