Diagnostica, Inc.
Diagnostica, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 2001.
Top product codes for Diagnostica, Inc.
Recent clearances by Diagnostica, Inc.
- K002756 — EASE-A-CULT
- K823348 — H. INFLUENZA B ANTISERA FOR CIE
- K812434 — DIAGNOSTIC KITS & KIT COMPONENTS
- K800398 — PARACONTROL ABNORMAL IMMUNOGLOBULIN CONT
- K791281 — ANTI-HUMAN IGG SERUM
- K791283 — ANTI-HUMAN LAMBDA SERUM
- K791284 — ANTI-HUMAN KAPPA SERUM
- K791282 — ANTI-HUMAN SERUM
- K791285 — ANTI-HUMAN GLOBULINS
- K790671 — DERMATOPHYTIN O
- K790672 — ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU
- K781710 — BUFFER, COLLAGEN REAGENT AND DILUENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.