BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)— 510(k) K903139

Substantially Equivalent

Siemens Medical Laboratories, Inc.

FDA 510(k) clearance K903139 for BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743), Substantially Equivalent on 1990-11-07. Applicant: Siemens Medical Laboratories, Inc..

Clearance details

Applicant: Siemens Medical Laboratories, Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 1990-07-17
Decision date: 1990-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

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.