Tina-Quant(R) Igm

FDA 510(k) K862762 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK862762

Submission

Device name
Tina-Quant(R) Igm
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
July 22, 1986
Decision date
September 8, 1986
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
K984326Elecys Ige AssayJHR · Traditional 02/08/1999SE
K983047Accu-Chek HQ SystemLFR · Traditional 02/05/1999SE
K984419Elecsys Ige CalcheckJJY · Traditional 02/02/1999SE
K984425Modification of Preciset Serum Proteins CalibratorJIX · Traditional 01/20/1999SE
K984372Elecsys Calcheck Troponin TJJY · Traditional 12/14/1998SE
K984105Elecsys Troponin T Stat TestMMI · Traditional 12/08/1998SE
K983503Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog…CEO · Traditional 12/01/1998SE
K983469Preciset Serum Proteins CalibratorJIX · Traditional 11/25/1998SE
K983185Boehringer Mannheim Tina-Quant Ige TestDGC · Traditional 11/12/1998SE
K983510Chemstrip 101 Urine AnalyzerKQO · Special 10/27/1998SE

Questions and answers

When was Tina-Quant(R) Igm cleared by the FDA?

Tina-Quant(R) Igm (K862762) received a 510(k) decision of Substantially Equivalent on September 8, 1986, 48 days after the submission was received.

What is the product code of K862762?

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