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510(k) K883836

COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-II by Coulter Immunology — Product Code GGK

K883836 is an FDA 510(k) premarket notification submitted by Coulter Immunology for the device "COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-II". The FDA issued a decision of Substantially Equivalent on November 30, 1988. The device falls under product code GGK (Products, Red-Cell Lysing Products), a Class I device regulated under 21 CFR 864.8540. Coulter Immunology has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 1988
Date Received
September 12, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Products, Red-Cell Lysing Products
Device Class
Class I
Regulation Number
864.8540
Review Panel
HE
Submission Type

Other clearances by Coulter Immunology

  • K922744 — CYTO-STAT/COULTER CLONE CD 3(IGG1)-FITC/T8-RD1 (February 5, 1993)
  • K922745 — CYTO-STAT/COULTER CLONE CD3(IGG1)-FITC/T4-RD1 (February 5, 1993)
  • K910473 — CYTO-STAT(R)/COULTER CLONE(R) T11-RD1/B4-FITC (October 31, 1991)
  • K911793 — COULTERCLONE (July 9, 1991)
  • K893853 — COULTER CLONE T8 MONOCLONAL ANTIBODY (March 2, 1990)
  • K893852 — COULTER CLONE T4 MONOCLONAL ANTIBODY (March 2, 1990)
  • K894179 — COULTER CLONE(R) MY4 MONOCLONAL ANTIBODY (February 12, 1990)
  • K895917 — CYTO-STAT/COULTER CLONE T4-RD1/T8-FITC MONO ANTI (December 29, 1989)
  • K884605 — COULTER CLONE MO2 (August 15, 1989)
  • K893419 — COULTER CLONE GAM-FITC POLY ANTI (IGG & IGM) (August 3, 1989)

Other clearances for product code GGK

  • K883991 — KVM HEMOGLOBIN LYSING REAGENT (October 12, 1988)
  • K874054 — FISHER DIAGNOSTICS HEMATALL III LAS REAGENT (October 20, 1987)
  • K873348 — CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG. (September 9, 1987)
  • K863114 — PIASTRINIT (November 6, 1986)
  • K863503 — HEMOLYSE (October 3, 1986)
  • K850944 — NSI LYSING-D REAGENT -4000 ML (March 29, 1985)
  • K850097 — LASER-LYSE (March 29, 1985)
  • K842938 — ACETIC ACID 1% V/V (September 14, 1984)
  • K842937 — ACETIC ACID 2% V/V (September 12, 1984)
  • K842936 — ACETIC ACID, 3% V/V (September 12, 1984)

FDA data resources