Hemotec, Inc.
Hemotec, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1990.
Top product codes for Hemotec, Inc.
Recent clearances by Hemotec, Inc.
- K902081 — CLOTTRAC(TM) IBEX HEPARINASE HR ACT CART./CONTROL
- K894317 — HEMOTEC HEPCON HMS COAGULATION SYSTEM & ACCESS.
- K894359 — CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS
- K894466 — HEPCON(R) CV WHOLE BLOOD COAGULATION CONTROLS
- K884590 — HEPCON/SYSTEM B-10 HEPARIN ASSAY/SCREEN/CARTRIDGES
- K875089 — HEPCON SYSTEM B-10 ACTIVATED CLOT TIME & HEPARIN
- K880302 — CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER
- K854376 — HEMOTEC CITRATED WHOLE BLOOD COAGULATION CONTROLS
- K854377 — HEMOTEC CV WHOLE BLOOD COAGULATION CONTROLS
- K853789 — ADDITIONAL HEMOTEC HEPCON/SYS B-10 COAGULATION CAR
- K843459 — HEMOTEC ACT I SYSTEM
- K841021 — HEMOTEC, HEPCON/SYS B-10 HEPARIN/PROTAM
- K830665 — HEPCOL SYSTEM B-10 & B-10-P
- K820410 — HEMOTEC HEPCON/SYSTEM FOUR & FOUR P
- K800161 — HEPCON/SYSTEM RC-10
Data sourced from openFDA. This site is unofficial and independent of the FDA.