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FDA product code NGG · Class 2 · Clinical Toxicology
2,140
Registered devices
0
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
Discover Plus — AMERICAN SCREENING, L.L.C.Discover — AMERICAN SCREENING, L.L.C.Discover Plus — AMERICAN SCREENING, L.L.C.Alltest MDMA500 Rapid Test Panel (Urine) — Hangzhou AllTest Biotech Co., Ltd.Discover — AMERICAN SCREENING, L.L.C.CLUNGENE — Hangzhou Clongene Biotech Co., Ltd.Alltest MDMA500 Rapid Test Dipstick(Urine)-CLIA Waived — Hangzhou AllTest Biotech Co., Ltd.Discover Plus — AMERICAN SCREENING, L.L.C.Precision Plus — AMERICAN SCREENING, L.L.C.Alltest Multi-Drug Rapid Urine Test Panel — Hangzhou AllTest Biotech Co., Ltd.Precision Plus — AMERICAN SCREENING, L.L.C.DrugCheck — Express Diagnostic Int'l, Inc.OneScreen — AMERICAN SCREENING, L.L.C.VeriCheck Drug Test Cup — Verify Diagnostics IncUScreen® — Instant Technologies, Inc.VeriCheck Drug Test Cup — Verify Diagnostics IncOneScreen — AMERICAN SCREENING, L.L.C.Discover — AMERICAN SCREENING, L.L.C.Reveal — AMERICAN SCREENING, L.L.C.Discover Plus — AMERICAN SCREENING, L.L.C.Discover Plus — AMERICAN SCREENING, L.L.C.Discover — AMERICAN SCREENING, L.L.C.iScreen™ — Instant Technologies, Inc.Discover — AMERICAN SCREENING, L.L.C.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-09-30 | Ameditech Inc | Product was released to market without the adulteration strip included in the product. |
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