Alfa Wassermann Diagnostic Technologies, Inc.
Alfa Wassermann Diagnostic Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2013.
Top product codes for Alfa Wassermann Diagnostic Technologies, Inc.
Recent clearances by Alfa Wassermann Diagnostic Technologies, Inc.
- K131975 — ACE DIRECT TOTAL IRON-BINDING CAPACITY (TIBC) REAGENT, ACE TOTAL IRON REAGENT, ACE LDH-L REAGENT
- K123953 — ACE CARBON DIOXIDE REAGENT, ACE DIRECT BILIUBIN REAGENT, ACE TOTAL BILIRUBIN REAGENT, ACE MAGNESIUM REAGENT
- K123018 — ACE ALERA CLINICAL CHEMISTRY SYSTEM, ACE GLUCOSE REAGENT, ACE ION SELECTIVE ELECTRODE (ISE) MODULE
- K122757 — ACE CHOLESTEROL REAGENT, ACE HDL-C REAGENT, ACE LDL-C REAGENT, ACE TRIGLYCERIDES REAGENT
- K113389 — ACE CK REAGENT,ACE BUN/UREA REAGENT,ACE URIC ACID REAGENT,ACE CREATININE REAGENT
- K113437 — ACE HEMOGLOBIN ALC(HBALC) REAGENT, ACE CEDIA T UPTAKE REAGENT, ACE T4 REAGENT, ACE FERRITIN REAGENT
- K113374 — ACE ALBUMIN REAGENT ACE TOTAL PROTEIN REAGENT ACE CALCIUM-ARSENAZO REAGENT ACE PHOSPHORUS U.V. REAGENT
- K113262 — ACE CHOLESTEROL REAGENT, ACE HDL-C REAGENT, ACE LDL-C REAGENT-C, ACE-TRISLYCERIDES REAGENT
- K113438 — ACE DIRECT TOTALIRON-BINDING CAPACITY (TIBC) REAGENT, ACE SERUM IRON REAGENT, ACE LIPASE REAGENT
- K113253 — ACE AXCEL CLINICAL CHEMISTRY SYSTEM,ACE ALBUMIN REAGENT,ACE TOTAL PROTEIN REAGENT,ACE BUN/UREANITROGEN REAGENT
- K112538 — ACE CHOLESTEROL REAGENT, ACE HDL-C REAGENT, ACE LDL-C REAGENT, ACE TRIGLYCERIDES REAGENT
- K103615 — ACE UREA NITROGEN REAGENT, CALCIUM-ARSEAZO REAGENT, CREATININE REAGENT, INORGANIC PHOSPHORUS U.V. REAGENT,URINE STANDARD
- K091711 — S- TEST HEMOGLOBIN ALC (HBA1C), MODEL RC0023
- K083040 — S-TEST C-REACTIVE PROTEIN (CRP)
- K082226 — S40 CREATINE KINASE (CK)
- K072143 — S40 CLINICAL ANALYZER, S TEST ALB
- K072142 — S40 CLINICAL ANALYZER, S TEST ALP, S TEST AMYLASE, S TEST AST
- K073223 — S-TEST C02
- K072140 — S40 CLINICAL ANALYZER, S TEST BIL, S TEST BUN, S TEST GLU
- K072141 — S40 CLINICAL ANALYZER, S TEST IP, S TEST UA
- K072356 — S-TEST CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.