Chrono-Log Corp.
Chrono-Log Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2016.
Top product codes for Chrono-Log Corp.
Recent clearances by Chrono-Log Corp.
- K161329 — Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channel
- K050265 — CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
- K032951 — CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A
- K962426 — CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592
- K945414 — RISTOCETIN COFACTOR ASSAY KIT
- K940792 — AGGRO/LINK VW COFACTOR SOFTWARE
- K932566 — AGGRO/LINK CONTROL SOFTWARE
- K922800 — PLATELET AGGREGATION REAGENTS
- K851025 — AGGRO/LINK COMPUTER INTERFACE
- K850592 — PLATELET AGGREGATION REAGENT
- K830749 — PLATELET AGGREGOMETER
- K820422 — PLATELET AGGREGOMETERS
- K781807 — REAGENT, FIREFLY #395
- K771198 — LUMI-AGGREGOMETER
- K760159 — AGGREGOMETER, DUAL CHANNEL PLATELET
- K760198 — KIT, PLATELET AGGREGATION REAGENT (#390)
Data sourced from openFDA. This site is unofficial and independent of the FDA.