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Redi-Check Photometer QC
AWARENESS TECHNOLOGY, INCORPORATED · Model Redi-Check Photometer QC · UDI-DI 00850229007119
10
510(k) clearances
0
Adverse events
2
Recalls
2
Facilities
Description
Photometer Quality Control
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-09-02 | Siemens Healthcare Diagnostics Inc | Error in the value assignment for the Chloride calibrators in the RAPIDPoint 400 and RAPIDPoint 405 Measurement Cartridge |
| 2016-09-02 | Siemens Healthcare Diagnostics Inc | Error in the value assignment for the Chloride calibrators in the RAPIDPoint 400 and RAPIDPoint 405 Measurement Cartridge |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
