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iScreen™

Instant Technologies, Inc. · Model ABTDUAK110701A · UDI-DI 00817405023486

NFTPTHNFVNFYNGGPTGNGLLCMNFW
1
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities

Description

10 PANEL 510(K) SQUARE CUP AMP1000, BAR300, BZO300, COC300, MDMA500, MET1000, MTD300, OPI2000, PCP25, THC50 SVT (CR,OX,SG)

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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.