FDA Device Intelligence
HomeAWARENESS TECHNOLOGY, INCORPORATED › Redi-Check Photometer QC

Redi-Check Photometer QC

AWARENESS TECHNOLOGY, INCORPORATED · Model Redi-Check Photometer QC · UDI-DI 00850229007119

JFS
10
510(k) clearances
0
Adverse events
2
Recalls
2
Facilities

Description

Photometer Quality Control

Recalls

DateFirmReason
2016-09-02Siemens Healthcare Diagnostics IncError in the value assignment for the Chloride calibrators in the RAPIDPoint 400 and RAPIDPoint 405 Measurement Cartridge
2016-09-02Siemens Healthcare Diagnostics IncError in the value assignment for the Chloride calibrators in the RAPIDPoint 400 and RAPIDPoint 405 Measurement Cartridge

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.