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ivWatch Patient Monitor

IVWATCH, LLC · Model Model 400 · UDI-DI 00814088020009

PMS Prescription
5
510(k) clearances
1
Adverse events
0
Recalls
2
Facilities

Description

A device to continuously monitor peripheral IVs for the early detection of IV infiltration and extravasation events

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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.