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510(k) K932463

BIOCLOT LA by Biopool AB — Product Code GIR

K932463 is an FDA 510(k) premarket notification submitted by Biopool AB for the device "BIOCLOT LA". The FDA issued a decision of Substantially Equivalent on September 27, 1993. The device falls under product code GIR (Reagent, Russel Viper Venom), a Class I device regulated under 21 CFR 864.8950. Biopool AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1993
Date Received
May 21, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Russel Viper Venom
Device Class
Class I
Regulation Number
864.8950
Review Panel
HE
Submission Type

Other clearances by Biopool AB

  • K941752 — SPECTROLYSE ANTIPLASMIN KIT (September 25, 1995)
  • K942087 — BIOPOOL VWF ELD KIT AND VWF ELD BULK PLATES (July 13, 1995)
  • K934314 — TINTELIZER(R) TPA (February 23, 1994)
  • K923499 — SPECTROLYSE HEPARIN KIT (January 27, 1994)
  • K920668 — MINUTEX D-DIMER LATEX TEST (October 16, 1992)
  • K922782 — SPECTROLYSE/PL PAI KIT (October 9, 1992)
  • K915163 — PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES (January 6, 1992)
  • K914307 — SPECTROLYSE PROTEIN C KIT (December 9, 1991)
  • K912025 — SPECTROLYSE PLASMINOGEN SK KIT (August 22, 1991)
  • K902530 — SPECTROLYSE ATIII KIT (August 9, 1990)

Other clearances for product code GIR

  • K132130 — REAGENT, RUSSEL VIPER VENOM - LA SCREEN (January 10, 2014)
  • K132076 — REAGENT, RUSSEL VIPER VENOM - LA CONFIRM (January 10, 2014)
  • K110031 — HEMOSIL DRVVT SCREEN & HEMOSIL DRVVT CONFIRM (August 24, 2011)
  • K083878 — LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA (June 25, 2010)
  • K061805 — STA - STACLOT DRVV SCREEN; STA - STACLOT DRVV CONFIRM (December 6, 2006)
  • K000527 — ACCUCLOT DRVVT SCREEN, CATALOG NO. A6094 (April 7, 2000)
  • K000528 — ACCUCLOT DRVVT CONFIRM, CATALOG NO. A62119 (April 7, 2000)
  • K990580 — CRYOCHECK LA SURE, MODEL SUR25-10 (July 28, 1999)
  • K990579 — CRYOCHECK LA CHECK, MODELS CHK25-10 (25 X1.0 ML), CHK80-10 (80 X 1.0 ML) (July 23, 1999)
  • K990302 — IL TEST LAC SCREEN (CLAIMS ADDED TO ACL FUTURA), IL TEST LAC CONFIRM (CLAIMS ADD (April 8, 1999)

FDA data resources