FDA Device Intelligence
Home › AMEDITECH INC. › ToxCup Drug Screen Cup

ToxCup Drug Screen Cup

AMEDITECH INC. · Model HT30 · UDI-DI 00816565020748

LCMDIODJCLDJDJGDKZ Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
95
Facilities

Description

AMP1000/COC300/MET1000/PCP25/THC50/OPI2000

Recalls

DateFirmReason
2005-05-31Applied Biotech IncThe 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 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.