FDA Device Intelligence
Home › DIAGNOSTIC HYBRIDS, INC. › D3 Fastpoint

D3 Fastpoint

DIAGNOSTIC HYBRIDS, INC. · Model 01-120000.B1 · UDI-DI 30014613330769

GQSOMGGNSLKTGNY Prescription
10
510(k) clearances
0
Adverse events
0
Recalls
5
Facilities

Description

D3 FASTPOINT LDFA VIR IDKIT BX

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.