Vitek Systems, Inc.
FDA 510(k) medical device clearances.
Top product codes for Vitek Systems, Inc.
Recent clearances by Vitek Systems, Inc.
- K920661 — VIDAS CMV IGG ASSAY
- K921302 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
- K921176 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
- K920952 — VITEK IMMUNODIAG ASSAY SYST(VIDAS) FERRITINE ASSAY
- K915884 — VIDAS CHLAMYDIA ASSAY, MODIFICATION
- K905211 — VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY
- K912371 — BIOMERIEUX RSV DIRECT IF KIT
- K910230 — LYME-SPOT IF KIT
- K910210 — SLIDEX MENINGITE-KIT 5
- K910304 — RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA
- K911429 — VITEK GRAM NEGATIVE IDENTIFICATION CARD, MODIFIED
- K910499 — IMMUNODIAGNOSTIC ASSAY SYSTEM HERPES SIMPLEX VIRUS
- K905787 — VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST
- K910666 — VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATION
- K895805 — SLIDEX ROTA-KIT 2
- K905020 — SLIDEX STREPTO-KIT
- K902925 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS) (RBG)
- K900996 — VITEK ANAEROBE IDENTIFICATION CARD
- K900818 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS) TOXO.
- K896097 — VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY
- K891385 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS)
- K883558 — VITEK GRAM-NEGATIVE IDENTIFICATION CARD
- K883279 — PHASE II FSH KIT
- K882252 — PHASE II LH KIT
- K881925 — VITEK YEAST BIOCHEMICAL CARD
- K843686 — AMS ANA CARD
- K842587 — GNC PLUS
- K834269 — AMS GRAM-NEGATIVE IDENT. CARD
- K834389 — AMS GRAM-POSITIVE IDENT. CARD
- K820264 — AMS GRAM-POSITIVE IDENTIFICATION CARD
- K792231 — AMS YEAST BIOCHEMICAL CARD
- K791932 — AMS ENTEROBACTERIACEASE CARE
- K782056 — CORD, ENTEROBACTERIACEAE BIOCHEMICAL
- K780731 — LIDOCAINE CALIBRATOR KIT
- K780960 — SERUM, CONTROL, DRUGS, ANTIARRYTHMIC
- K780961 — THEOPHYLLINE CONTROL SERUM
- K780732 — PROCAINAMIDE CALIBRATOR KIT
- K780733 — ANTICONVULSANTS III CALIBRATOR KIT
- K780734 — ANTICONVULSANTS II CALIBRATOR KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.