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NuFLO2 Hyperinflation System

MERCURY ENTERPRISES, INC. · Model 10-56807 · UDI-DI 10641043568071

NHK Prescription
1
510(k) clearances
113
Adverse events (6 deaths)
0
Recalls
9
Facilities

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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.