Home › Instant Technologies, Inc. › iScreen™
iScreen™
Instant Technologies, Inc. · Model ABTDUAW114704D · UDI-DI 00817405023882
10
510(k) clearances
5
Adverse events
1
Recalls
95
Facilities
Description
14 Panel CLIA Waived Click Cup w/ SVT AMP1000, BAR300, BUP10, BZO300, COC300, MDMA500, MET1000, MTD300, OPI2000, OXY100, PCP25, PPX300, TCA1000, THC50 w/ SVT OX/SG/pH
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.