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Argyle

Cardinal Health, Inc. · Model 8881450004 · UDI-DI 10884521020337

DYN
10
510(k) clearances
100
Adverse events (1 deaths)
0
Recalls
151
Facilities

Description

Saliva Ejector Flexible Lightweight Vinyl

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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.