Rapid Response
BTNX Inc · Model D3.36-1V · UDI-DI 00722066005309
1
510(k) clearances
0
Adverse events
0
Recalls
50
Facilities
Description
3 Panel One Step DOA Cup(3.36) - COC300 AMP1000 MET1000
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 docsData 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.