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510(k) K843459

HEMOTEC ACT I SYSTEM by Hemotec, Inc. — Product Code JBP

K843459 is an FDA 510(k) premarket notification submitted by Hemotec, Inc. for the device "HEMOTEC ACT I SYSTEM". The FDA issued a decision of Substantially Equivalent on December 12, 1984. The device falls under product code JBP (Activated Whole Blood Clotting Time), a Class II device regulated under 21 CFR 864.7140. Hemotec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 12, 1984
Date Received
September 5, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Activated Whole Blood Clotting Time
Device Class
Class II
Regulation Number
864.7140
Review Panel
HE
Submission Type

Other clearances by Hemotec, Inc.

  • K902081 — CLOTTRAC(TM) IBEX HEPARINASE HR ACT CART./CONTROL (July 3, 1990)
  • K894317 — HEMOTEC HEPCON HMS COAGULATION SYSTEM & ACCESS. (September 5, 1989)
  • K894359 — CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS (September 5, 1989)
  • K894466 — HEPCON(R) CV WHOLE BLOOD COAGULATION CONTROLS (September 5, 1989)
  • K884590 — HEPCON/SYSTEM B-10 HEPARIN ASSAY/SCREEN/CARTRIDGES (January 10, 1989)
  • K875089 — HEPCON SYSTEM B-10 ACTIVATED CLOT TIME & HEPARIN (March 9, 1988)
  • K880302 — CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER (February 19, 1988)
  • K854376 — HEMOTEC CITRATED WHOLE BLOOD COAGULATION CONTROLS (December 4, 1985)
  • K854377 — HEMOTEC CV WHOLE BLOOD COAGULATION CONTROLS (December 4, 1985)
  • K853789 — ADDITIONAL HEMOTEC HEPCON/SYS B-10 COAGULATION CAR (October 4, 1985)

Other clearances for product code JBP

  • K223635 — Sonoclot Coagulation & Platelet Function Analyzer System with Sonoclot Viewer (January 4, 2023)
  • K062604 — RAPIDTEG TEG-ACT TEST (January 31, 2007)
  • K032952 — AIACT KIT (December 12, 2003)
  • K023582 — I-STAT KAOLIN ACT TEST (September 8, 2003)
  • K020914 — ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, MODEL 5770 (May 23, 2002)
  • K013078 — ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM, MODEL 5750/5752 (January 10, 2002)
  • K002528 — SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER SYSTEM WITH SIGNATURE VIEWER O (August 31, 2000)
  • K994194 — (TAS) LOW RANGE HEPARIN MANAGEMENT CARD RAPIDPOINT (March 28, 2000)
  • K992571 — I-STAT SYSTEM (February 10, 2000)
  • K992851 — ACT TEST CATRIDGES FOR COAGUCHEK PRO SYSTEM, ACT CONTROLS FOR COAGUCHEK PRO SYST (January 14, 2000)

FDA data resources