Vitek Systems, Inc.
Vitek Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1993.
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.