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510(k) K880302

CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER by Hemotec, Inc. — Product Code GGN

K880302 is an FDA 510(k) premarket notification submitted by Hemotec, Inc. for the device "CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER". The FDA issued a decision of Substantially Equivalent on February 19, 1988. The device falls under product code GGN (Plasma, Coagulation Control), a Class II device regulated under 21 CFR 864.5425. Hemotec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 19, 1988
Date Received
January 25, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plasma, Coagulation Control
Device Class
Class II
Regulation Number
864.5425
Review Panel
HE
Submission Type

Other clearances by Hemotec, Inc.

  • K902081 — CLOTTRAC(TM) IBEX HEPARINASE HR ACT CART./CONTROL (July 3, 1990)
  • K894466 — HEPCON(R) CV WHOLE BLOOD COAGULATION CONTROLS (September 5, 1989)
  • K894317 — HEMOTEC HEPCON HMS COAGULATION SYSTEM & ACCESS. (September 5, 1989)
  • K894359 — CLOTRAC CITRATED 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)
  • 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)
  • K843459 — HEMOTEC ACT I SYSTEM (December 12, 1984)

Other clearances for product code GGN

  • K170864 — VALIDATE D-Dimer Calibration Verification / Linearity Test Kit (June 21, 2017)
  • K163498 — VALIDATE Heparin Calibration Verification/Linearity Test Kit (March 16, 2017)
  • K161316 — George King Coumadin Plasma (February 23, 2017)
  • K162705 — VALIDATE® D-Dimer Calibration Verification/ Linearity Test Kit (January 5, 2017)
  • K152961 — VALIDATE D-Dimer Calibration Verification/Linearity Test Kit (June 3, 2016)
  • K150144 — VisuCon-F Low Fibrinogen Control Plasma (March 6, 2016)
  • K142132 — POOL NORM (December 12, 2014)
  • K133582 — HEMOSIL D-DIMER HS 500 CONTROL (August 15, 2014)
  • K120977 — DIRECTCHECK CONTROL FOR HEMOCHRON JR. MICROCOAGULATION SYSTEMS ACT-LR CUVETTE DI (July 3, 2013)
  • K120900 — I-STAT PT CONTROL LEVIEL 1 I-STAT PT CONTROL LEVEL 2 (May 31, 2013)

FDA data resources