FDA Device Intelligence
HomeBIO CENTRIC INC. › Bio Centric Inc

Bio Centric Inc

BIO CENTRIC INC. · Model BP900SiM · UDI-DI 00860005485802

NPP
1
510(k) clearances
10
Adverse events
0
Recalls
2
Facilities

Description

Cellular enabled Class II BP Monitor

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.