Rapid Response
BTNX Inc · Model D7.17-1P29-25 · UDI-DI 00722066004791
1
510(k) clearances
2
Adverse events
0
Recalls
51
Facilities
Description
7-Drug Test Panel - 25/Kit (7.17) - COC300 MET1000 MOP300 OPI2000 OXY100 BZO300 BUP10
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.