Syn-Kit, Inc.
Syn-Kit, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1986.
Top product codes for Syn-Kit, Inc.
Recent clearances by Syn-Kit, Inc.
- K861098 — SEROIDEN STREPTO KIT 'EIKEN'
- K861631 — SLIDE CULTURE U 'EIKEN'
- K854819 — CPR SLIDE EIKEN
- K854820 — RA 80 EIKEN
- K853276 — ASO SLIDE EIKEN
- K843753 — UROPAPER EIKEN GP
- K843754 — UROPAPER EIKEN 7
- K843755 — UROPAPER EIKEN 6B
- K843756 — UROPAPER EIKEN 5
- K843757 — UROPAPER EIKEN AG
- K843758 — UROPAPER EIKEN GK
- K843759 — UROPAPER EIKEN HAG
- K843760 — UROPAPER EIKEN G
- K843532 — UROPAPER EIKEN 8
- K833521 — REAGENT TESTS STRIP COMBINATIONS
- K830824 — URINE SCREENING KIT
- K821167 — URICASE (U.V.) URIC ACID
- K821105 — CHOLESTEZYME-V EIKEN
- K821106 — TRIGLYZYME V EIKEN
- K820567 — TREP CARD EIKEN
- K813164 — SYSTEK #1 EIKEN
- K812298 — FIBROGEN(FIBRIN SPLIT PRODUCT) ANTIGEN
- K811815 — UROPAPER EIKEG
- K811816 — UROPAPER EIKEN UHAG
- K813192 — HDL-C EIKEN
- K811818 — UROPAPER EIKEN UAG
- K811817 — UROPAPER EIKEN AG
- K802447 — GOT ISOENZYME ASSAY EIKEN KIT
- K810862 — CRP SLIDE
- K802451 — BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.
- K802448 — RA 80 EIKEN KIT DETERM. OF RHEUMATIC F.
- K802452 — TOXOTEST-MT EIKEN KIT
- K802454 — GESTE FOLLOW KIT DETERM. OF HPL
- K802450 — GESTATE SLIDE EIKEN KIT AGG. METHOD HUM
Data sourced from openFDA. This site is unofficial and independent of the FDA.