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Argyle

Cardinal Health, Inc. · Model MI00775 · UDI-DI 10884527006458

BTX
10
510(k) clearances
5
Adverse events
0
Recalls
16
Facilities

Description

I.V. Support Board,Small

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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.