Home › Inogen, Inc. › TUB10
TUB10
Inogen, Inc. · Model TUB10 · UDI-DI 36642240000232
SDT
Prescription
3
510(k) clearances
0
Adverse events
0
Recalls
9
Facilities
Description
1 single patient use expiratory kit, composed of 1 tube, 1 filter programmed to allow 10 therapy sessions and 10 disposable mouthpieces
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 docsData 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.
