FDA Device Intelligence
HomeByFlo LLC › ByFloProducts

ByFloProducts

ByFlo LLC · Model BFP50D1 · UDI-DI 00628693098045

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

Description

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.