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Intercept i2 Oral Fluid Collection Device

Orasure Technologies, Inc. · Model 3001-2661 · UDI-DI 00608337000917

NNK Prescription
0
510(k) clearances
18
Adverse events
0
Recalls
189
Facilities

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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.