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AGFA CPB 200

AGFA · Model AGFA CPB 200 13X18 · UDI-DI 05414904037232

IXA Prescription
1
510(k) clearances
11
Adverse events
1
Recalls
16
Facilities

Description

AGFA CP CASSETTE / AGFA CPB 200

Recalls

DateFirmReason
2005-01-26AGFA Corp.Users of these cassettes may detect poor film to screen contact and unsatisfactory sharpness of radiographic images.

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

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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.