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AMERICAN SCREENING, L.L.C. · Model DIS-DBU-114 · UDI-DI 00840050504147

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

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.