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510(k) K844708

TRI-COUNT CALIBRATOR by Hematology Marketing Assoc. — Product Code KSA

K844708 is an FDA 510(k) premarket notification submitted by Hematology Marketing Assoc. for the device "TRI-COUNT CALIBRATOR". The FDA issued a decision of Substantially Equivalent on March 5, 1985. The device falls under product code KSA (Calibrator For Red-Cell And White-Cell Counting), a Class II device regulated under 21 CFR 864.8185. Hematology Marketing Assoc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1985
Date Received
December 3, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator For Red-Cell And White-Cell Counting
Device Class
Class II
Regulation Number
864.8185
Review Panel
HE
Submission Type

Other clearances by Hematology Marketing Assoc.

  • K851843 — OSMOCEL 3 (July 30, 1985)
  • K851375 — TRI-COUNT (July 12, 1985)
  • K850097 — LASER-LYSE (March 29, 1985)
  • K850095 — LASER-DIL (March 29, 1985)
  • K850094 — LASER-GLOBIN POWDER (March 29, 1985)
  • K850096 — LASER-GLOBIN (March 29, 1985)
  • K843485 — TRI-COUNT LASER (December 12, 1984)
  • K834371 — TRI-COUNT 10 (March 9, 1984)
  • K833130 — TRI-COUNT 7 (October 20, 1983)
  • K831306 — HEMACAL (June 16, 1983)

Other clearances for product code KSA

  • K943268 — SCS-1000 (SYSMEX CALIBRATOR SYSTEM) (December 15, 1994)
  • K897060 — CBC-CAL(TM) PLUS HEMATOLOGY CALIBRATOR/MULTIPLE (January 2, 1990)
  • K881161 — TECH-CAL(TM)/MULTIPLE (May 2, 1988)
  • K864664 — H-1 SETPOINT PLATELET AND RBC/WBC CALIBRATORS (February 6, 1987)
  • K854823 — CBC-CAL/MULTIPLE (February 13, 1986)
  • K813530 — HEMOTOLOGY CALIBRATOR (February 22, 1982)
  • K813375 — HEMATOLOGY CALIBRATOR S-CAL (February 4, 1982)

FDA data resources