FDA Device Intelligence
Home › VASOMEDICAL, INC. › Hose, Complete Set, Calf, Upper Thigh & Lower Thigh (AngioNew® V)

Hose, Complete Set, Calf, Upper Thigh & Lower Thigh (AngioNew® V)

VASOMEDICAL, INC. · Model Model AngioNew V · UDI-DI 00817980021280

DRN Prescription
1
510(k) clearances
58
Adverse events (6 deaths)
1
Recalls
8
Facilities

Description

Hose, Complete Set, Calf, Upper Thigh & Lower Thigh (AngioNew® V)

Recalls

DateFirmReason
2009-04-09Cardiomedics IncorporatedCuff may underinflate, or device may stop working during use. Cardioassist software version 4.3.1 utilized a signal from the plethysmograph that was found not to be sensitive enou

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.