Trace America, Inc.
Trace America, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2001.
Top product codes for Trace America, Inc.
Recent clearances by Trace America, Inc.
- K003583 — LITHIUM REGENT MODEL TR66056 / LITHIUM STANDARD TR66901
- K980026 — GLUCOSE (HK) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
- K980028 — ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
- K980030 — AST )GOT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
- K973869 — TRACE REAGENT LINE FOR THE COBAS MIRA
- K974620 — AMMONIA-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
- K972297 — AMYLASE-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
- K971477 — UREA (UREA NITROGEN) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
- K971485 — URIC ACID - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
- K962723 — TRACE HDL CHOLESTEROL - AUTOMATED (HOMOGEN
- K961984 — PORPHOBILINOGEN (PBG)
- K961477 — TRIGLYCERIDES - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY
- K960035 — CARBON DIOXIDE - DST
- K953971 — TRIGLYCERIDES LIQUID STABLE INCORPORATING DYNAMIC STABILISATION TECHNOLOGY
- K952410 — CARBON DIOXIDE - DST
- K925794 — TRACE MICROPROTEIN REAGENT
- K920603 — TRACE MAGNESIUM - ARSENAZO REAGENT
- K895381 — HDL SINGLES
- K880794 — RESUBMITTED BICARBONATE (CO2) REAGENT SINGLE VIAL
- K880795 — RESUBMITTED ALKALINE PHOSPHATASE REAGENT AMP BUFF.
- K880796 — ALKALINE PHOSPHATASE REAGENT, DEA BUFF
- K880798 — ACID PHOSPHATASE REAGENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.