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Ventlab

VENTLAB, LLC · Model HS4041-B · UDI-DI 10889483113226

NHK Prescription
10
510(k) clearances
118
Adverse events (6 deaths)
0
Recalls
9
Facilities

Description

1/4 LITER HYPER SYSTEM W/MANOMETER & 7' SALTER TUBING

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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.