FDA Device Intelligence
Home › Drive Devilbiss Healthcare › Winner EVO Combo

Winner EVO Combo

Drive Devilbiss Healthcare · Model 210-010-220 · UDI-DI 00852515007735

IMGIMIIPFGZJLIH
1
510(k) clearances
235
Adverse events (2 deaths)
2
Recalls
24
Facilities

Description

Winner EVO-CM2, 220v

Recalls

DateFirmReason
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.

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.