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RDS

AMERICAN BIO MEDICA CORPORATION · Model 10-7SP-306 · UDI-DI 10694644300526

LFI LDJ LCM JXM DJG DJC DIS DIO DZK Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

7P RDS/5MO+MTD AMP op3 single

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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.