Home › SYNTRON BIORESEARCH, INC. › QuikScreen 13+4 Drug Cup Test
QuikScreen 13+4 Drug Cup Test
SYNTRON BIORESEARCH, INC. · Model 65D03-17 · UDI-DI 00748349000038
10
510(k) clearances
5
Adverse events
1
Recalls
94
Facilities
Description
QuikScreen 13+4 (pouch cup): AMP 1000, BAR 300, BUP 10, BZD 300, COC 300, MAD 300, MDMA 500, MET 1000, MDMA 500, OPI 300, OXY 100, PCP 25, THC 50 + pH/CRE/SG/GTA
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-05-31 | Applied Biotech Inc | The firm has discovered that a number of distributed devices of the Medplus ER Drug Screen Test may be incorrectly assembled which may give incorrect results. The product is an in |
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.