CURIX ORTHO REGULAR
AGFA · Model CURIX ORTHO REGULAR 35X35 · UDI-DI 05414904036693
IXA
Prescription
1
510(k) clearances
11
Adverse events
1
Recalls
16
Facilities
Description
CURIX CAS US+OR REG 35X35
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-01-26 | AGFA Corp. | Users of these cassettes may detect poor film to screen contact and unsatisfactory sharpness of radiographic images. |
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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.