American Diagnostica, Inc.
American Diagnostica, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2008.
Top product codes for American Diagnostica, Inc.
Recent clearances by American Diagnostica, Inc.
- K080069 — DIMERTEST
- K063323 — SPECTROLYSE PAI-1, MODEL 101201
- K052124 — ACTICLOT, MODEL 824
- K013637 — ACTICHROME HEPARIN (ANTI-FIIA)
- K013492 — IMUBIND TPA ELISA, MODEL 860
- K013318 — ACTICHROME HEPARIN (ANTI-FXA), MODEL 832
- K013168 — IMUBIND PLASMA PAI-1 ELISA,MODEL 822
- K012386 — ACTICLOT PROTEIN S, MODEL 843L
- K940490 — DV TEST AND DVV CONFIRM
- K935254 — DVVTEST AND DVVCONFIRM LUPUS ANTICOAGULANT NORMAL AND ABNORMAL CONTROL PLASMA
Data sourced from openFDA. This site is unofficial and independent of the FDA.