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Connecticut Diagnostics, Ltd.

FDA 510(k) & PMA Approved Devices — 14 products

Total Devices14
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K905617 VISI-STAPHJWX1991-03-29 View
510(k) K822504 CDL AUTO-LYSING REAGENTGGK1982-09-17 View
510(k) K822501 CDL ISOTONIC DILUENTGIF1982-09-17 View
510(k) K822500 CDL LYSING REAGENTGGK1982-09-17 View
510(k) K811222 INORGANIC PHOSPHORUS REAGENTSCED1981-05-21 View
510(k) K801897 GLUCOSE DIAGNOSTIC REAGENTCGA1980-10-10 View
510(k) K801898 URIC ACID DIAGNOSTIC REAGENTKNK1980-10-10 View
510(k) K792465 CONNECTICUT DIAGNOSTICS, LTS. DIRECTCIG1979-12-18 View
510(k) K792362 BLOOD UREA NITROGEN REAGENTJGZ1979-12-06 View
510(k) K792339 CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGENCIX1979-12-06 View
510(k) K792338 DONNECT. DIAG. TOTAL BILIRUBIN REAGENTSCIG1979-12-06 View
510(k) K792337 DONNECT. DIAG. CALCIUM DIAG. REAGENTCIC1979-12-06 View
510(k) K792340 CONNECT. DIAG. TOTAL PROTEIN DIAG. REAGECEK1979-12-06 View
510(k) K791994 CREATININE DIAG. REAGENT PICRIC ACIDCGX1979-10-17 View
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