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510(k) K800310

ORTHO ANTISERA CONTROL by Ortho Diagnostics, Inc. — Product Code KSF

K800310 is an FDA 510(k) premarket notification submitted by Ortho Diagnostics, Inc. for the device "ORTHO ANTISERA CONTROL". The FDA issued a decision of Substantially Equivalent on March 5, 1980. The device falls under product code KSF (Kit, Quality Control For Blood Banking Reagents), a Class II device regulated under 21 CFR 864.9650. Ortho Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1980
Date Received
February 12, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Quality Control For Blood Banking Reagents
Device Class
Class II
Regulation Number
864.9650
Review Panel
HE
Submission Type

Other clearances by Ortho Diagnostics, Inc.

  • K802404 — ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE (October 23, 1980)
  • K801507 — ANTIGEN CONTROL CELLS (August 20, 1980)
  • K800357 — BI-LEVEL ASSAYED CARD. DRUG CONT., I,II (April 16, 1980)
  • K791791 — ORTHO ANTIBODY ENHANCEMENT SOLUTION (October 11, 1979)
  • K791301 — ORTHO TSH RIA KIT (September 24, 1979)
  • K790813 — MULTECON BLOOD GAS CONTROL (June 28, 1979)
  • K782166 — SLIDE TEST FOR PREGNANCY, GRAVINDEX 90 (April 4, 1979)
  • K782063 — PREGNANCY, SENSIDEX TUBE TEST (April 4, 1979)
  • K781638 — RUBINDEX*DIRECT SYSTEM (December 20, 1978)
  • K781860 — ASSAY, CHROMOGENIC ANTITHROMBIN III (December 4, 1978)

Other clearances for product code KSF

  • K811713 — AVI-D CONTROL (October 23, 1981)
  • K810599 — DADE RH CONTROL REAGENT (March 31, 1981)
  • K801425 — RH CONTROL (July 14, 1980)
  • K800658 — RST-SERIES CONTROL (April 16, 1980)
  • K800239 — RH-HR NEGATIVE CONTROL REAGENT (February 21, 1980)
  • K790249 — TEST CELLS (May 16, 1979)
  • K790025 — COUNTER CHECK, H001, H002, H003 (January 17, 1979)
  • K780665 — RECAP (June 6, 1978)
  • K780097 — QUALITY CONTROL SYSTEM, SPECTRA (April 24, 1978)
  • K771814 — REAGENT CONFIDENCE SERA (November 7, 1977)

FDA data resources