Tia-Igm Reagent & Calibrator Sets

FDA 510(k) K831103 · Worthington Diagnostic Systems

Substantially Equivalent

510(k) numberK831103

Submission

Device name
Tia-Igm Reagent & Calibrator Sets
Applicant
Worthington Diagnostic Systems
Mchenry, IL, US
Received
April 5, 1983
Decision date
April 27, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DFT – Igm, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5550
Specialty
Immunology

Other 510(k)s with product code DFT

510(k)DeviceApplicantDecision
K983132IgmDFT · Traditional Abbott Laboratories11/04/1998SE
K962201Quantex IgmDFT · Traditional Instrumentation Laboratory CO09/25/1996SE
K955797Igm Immunotrubidimetric & CalibratorDFT · Traditional Randox Laboratories, Ltd.04/05/1996SE
K945522I.D.-Zone Immunofixation Electrophoresis ControlsDFT · Traditional Beckman-Diagnostic Systems Group12/12/1994SE
K901453Quik-Sep(R) Igm Rprotein G Affinity MethodDFT · Traditional Isolab, Inc.04/12/1990SE
K894417Raichem(Tm) Spia(Tm) Igm ReagentsDFT · Traditional Reagents Applications, Inc.08/02/1989SE
K884147Immunochemical Determination of Immunoglobulin MDFT · Traditional Orion Diagnostica, Inc.10/27/1988SE
K880828Wako(Tm) Igm-Ha DirectDFT · Traditional Wako Chemicals USA, Inc.03/25/1988SE
K873871Immunoglobulins MDFT · Traditional Unipath , Ltd.10/13/1987SE
K872237Kallestad QM300 Igm Antibody PackDFT · Traditional Kallestad Diag, A Div. of Erbamont, Inc.07/09/1987SE

More from Kallestad Diag, A Div. of Erbamont, Inc.

510(k)DeviceDecision
K833708Compur* M1000 Hemoglobin & ErythrocyteLKZ · Traditional 01/04/1984SE
K832785Compur* Easy Touch Uric Acid ReagentKNK · Traditional 10/14/1983SE
K832749Easytouch Bun Reagent SetCDQ · Traditional 10/14/1983SE
K832748Compur* Easytouch Total BilirubinCIG · Traditional 10/14/1983SE
K832427Easytouch Tromboplastin ReagentGJS · Traditional 10/14/1983SE
K832750Easytouch Hemoglobin ReagentKHG · Traditional 09/26/1983SE
K832426Easytouch Triglycerides Reagent SetCDT · Traditional 09/12/1983SE
K831477Demand Analyzer SystemJJE · Traditional 06/17/1983SE
K831318Compur* M1100 Hematrcrit SystemJPI · Traditional 06/08/1983SE
K831227Compur Easy Touch Chemistry Analyzer-JJF · Traditional 06/02/1983SE

Questions and answers

When was Tia-Igm Reagent & Calibrator Sets cleared by the FDA?

Tia-Igm Reagent & Calibrator Sets (K831103) received a 510(k) decision of Substantially Equivalent on April 27, 1983, 22 days after the submission was received.

What is the product code of K831103?

The FDA product code is DFT – Igm, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5550.