FDA Device Intelligence
Home › VENTLAB, LLC › Ventlab

Ventlab

VENTLAB, LLC · Model HS4051-M0-00 · UDI-DI 10889483100714

NHK Prescription
10
510(k) clearances
113
Adverse events (6 deaths)
0
Recalls
9
Facilities

Description

1/2 LITER HYPER SYSTEM W/MANOMETER AND 2 MASKS

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.