FDA Device Intelligence
Home › COMPASS HEALTH BRANDS CORP. › Carex

Carex

COMPASS HEALTH BRANDS CORP. · Model FGR41800 0000 · UDI-DI 00023601064189

OCH
0
510(k) clearances
35
Adverse events
0
Recalls
58
Facilities

Description

Fingertip Pulse Oximeter

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.