Home / 510(k) Clearances / K924733

510(k) K924733

ETHYL ALCOHOL CALIBRATORS & CONTROL by Diagnostic Reagents, Inc. — Product Code DNN

K924733 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "ETHYL ALCOHOL CALIBRATORS & CONTROL". The FDA issued a decision of Substantially Equivalent on December 9, 1992. The device falls under product code DNN (Calibrators, Ethyl Alcohol), a Class II device regulated under 21 CFR 862.3200. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 9, 1992
Date Received
September 22, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrators, Ethyl Alcohol
Device Class
Class II
Regulation Number
862.3200
Review Panel
TX
Submission Type

Other clearances by Diagnostic Reagents, Inc.

  • K983268 — MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY (November 18, 1998)
  • K983812 — NAPA EIA ASSAY (November 16, 1998)
  • K983323 — DIGOXIN IMMUNOASSAY (November 12, 1998)
  • K983280 — VANCOMYCIN EIA ASSAY (November 6, 1998)
  • K983159 — DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLS (November 5, 1998)
  • K973102 — LIDOCAINE EIA ASSAY (September 12, 1997)
  • K972835 — 50NG/ML COCAINE METABOLITE CALIBRATOR (August 28, 1997)
  • K972526 — METHADONE EIA ASSAY (August 4, 1997)
  • K964212 — QUINIDINE ENZYME IMMUNOASSAY (December 18, 1996)
  • K963835 — DIGOXIN ENZYME IMMUNOASSAY (December 10, 1996)

Other clearances for product code DNN

  • K990516 — ETHYL ALCOHOL CLINICAL STANDARD SOLUTIONS (March 31, 1999)
  • K973054 — ETHYL ALCOHOL CLINICAL STANDARD SOLUTIONS (October 1, 1997)
  • K882117 — ETHYL ALCOHOL STANDARD (August 4, 1988)
  • K853532 — ALCOHOL CALIBRATORS (September 16, 1985)
  • K810466 — ETHYL ALCOHOL SERUM CALIBRATOR (March 6, 1981)
  • K802620 — EMIT-STM ETHYL ALCOHOL URINE CALIBRATOR (October 31, 1980)

FDA data resources