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510(k) K810296

DIGOXIN RIA ASSAY by Ria Diagnostics — Product Code DON

K810296 is an FDA 510(k) premarket notification submitted by Ria Diagnostics for the device "DIGOXIN RIA ASSAY". The FDA issued a decision of Substantially Equivalent on February 19, 1981. The device falls under product code DON (Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.), a Class II device regulated under 21 CFR 862.3320. Ria Diagnostics has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 19, 1981
Date Received
February 4, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.
Device Class
Class II
Regulation Number
862.3320
Review Panel
TX
Submission Type

Other clearances by Ria Diagnostics

  • K855033 — T-3 UPTAKE/RIASSAY (January 24, 1986)
  • K854798 — T-4 RIASSAY (January 15, 1986)
  • K852537 — T-3 RIASSAY (August 12, 1985)
  • K801691 — TSH RIASSAY (August 27, 1980)
  • K792062 — THEOPHYLLINE RIASSAY (February 25, 1980)
  • K780012 — ANTITHROMBIN III RIA (January 20, 1978)

Other clearances for product code DON

  • K902861 — CIBA CORNING ACS DIGOXIN IMMUNOASSAY (September 10, 1990)
  • K881679 — CIBA CORNING MAGIC LITE DIGOXIN IMMUNOASSAY (July 8, 1988)
  • K840461 — MAGIC 125I DIGOXIN RADIOIMMUNOASSAY (March 23, 1984)
  • K830533 — PHASE II DIGOXIN RADIOIMMUNOASSAY KIT (April 5, 1983)
  • K822053 — ZETAPHASE-DIG (July 27, 1982)
  • K821000 — ENZYMUNE-TEST DIGOXIN (April 26, 1982)
  • K803075 — DIGOXIN RIABEAD DIAGNOSTIC KIT (December 22, 1980)
  • K791549 — TECHNICON STAR SYSTEM (September 27, 1979)
  • K781660 — RIA, DIGOXIN (October 24, 1978)
  • K780475 — DAC-CEL DIGOXIN RADIOIMMUNOASSAY KIT (April 24, 1978)

FDA data resources