Abaxis, Inc.
Abaxis, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2021, with 1 FDA device recall on record.
Top product codes for Abaxis, Inc.
FDA recalls by Abaxis, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Abaxis, Inc.
- K200865 — Piccolo Potassium Test System
- K130113 — PICCOLO LACTATE TEST SYSTEM
- K130200 — PICCOLO TOTAL CHOLESTEROL - CAPILLARY TEST SYSTEM
- K120662 — PICCOLO HDL-CAPILLARY TEST SYSTEM
- K120664 — PICCOLO TRGLYCERIDES-CAPILLARY TEST SYSTEM
- K091052 — PICCOLO C-REACTIVE PROTEIN (CRP) TEST SYSTEM
- K091910 — PICCOLO MAGNESIUM TEST SYSTEM
- K051108 — PICCOLO LACTATE DEPHYDROGENASE TEST SYSTEM
- K040115 — PICCOLO MAGNESIUM TEST SYSTEM
- K023639 — PICCOLO TRIGLYCERIDES TEST SYSTEM
- K023640 — PICCOLO HDL TEST SYSTEM
- K023642 — PICCOLO TOTAL CHOLESTEROL TEST SYSTEM
- K022312 — PICCOLO PHOSPHORUS TEST SYSTEM
- K010670 — PICCOLO CHLORIDE TEST SYSTEM
- K993211 — PICCOLO SODIUM TEST SYSTEM
- K992140 — PICCOLO METLYTE 7 REAGENT DISC
- K955770 — GAMMA GLUTAMYL TRANSFERASE TEST SYSTEM
- K950164 — PICCOLO(TM) PRIMARY HEALTH PANEL REAGENT ROTOR
- K942782 — PICCOLO(TM)
- K934592 — EPOC 2000 POINT-OF-CARE ANALYZER AND EPOC 5-CHEMISTRY REAGENT ROTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.