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Multi-Drug 13 Drugs Rapid Test Cup

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16936983197240

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1
510(k) clearances
0
Adverse events
1
Recalls
52
Facilities

Description

25T, FDA Clia Waived, MOP(OPI)300/MDMA500/OXY100/PCP25/MTD300/BAR300/BZO300/COC300/AMP1000/MET1000/THC50/BUP10/FYL1

Recalls

DateFirmReason
2017-09-30Ameditech IncProduct was released to market without the adulteration strip included in the product.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.