I.D.-Zone Immunofixation Electrophoresis Controls
FDA 510(k) K945522 · Beckman-Diagnostic Systems Group
510(k) numberK945522
Submission
- Device name
- I.D.-Zone Immunofixation Electrophoresis Controls
- Applicant
- Beckman-Diagnostic Systems Group
Brea, CA, US - Received
- November 10, 1994
- Decision date
- December 12, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K983132 | IgmDFT · Traditional | Abbott Laboratories | 11/04/1998SE |
| K962201 | Quantex IgmDFT · Traditional | Instrumentation Laboratory CO | 09/25/1996SE |
| K955797 | Igm Immunotrubidimetric & CalibratorDFT · Traditional | Randox Laboratories, Ltd. | 04/05/1996SE |
| K901453 | Quik-Sep(R) Igm Rprotein G Affinity MethodDFT · Traditional | Isolab, Inc. | 04/12/1990SE |
| K894417 | Raichem(Tm) Spia(Tm) Igm ReagentsDFT · Traditional | Reagents Applications, Inc. | 08/02/1989SE |
| K884147 | Immunochemical Determination of Immunoglobulin MDFT · Traditional | Orion Diagnostica, Inc. | 10/27/1988SE |
| K880828 | Wako(Tm) Igm-Ha DirectDFT · Traditional | Wako Chemicals USA, Inc. | 03/25/1988SE |
| K873871 | Immunoglobulins MDFT · Traditional | Unipath , Ltd. | 10/13/1987SE |
| K872237 | Kallestad QM300 Igm Antibody PackDFT · Traditional | Kallestad Diag, A Div. of Erbamont, Inc. | 07/09/1987SE |
| K871498 | Titan Gel Immunofix ControlsDFT · Traditional | Helena Laboratories | 04/29/1987SE |
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| K936184 | Vigil PRX Chemistry ControlJJY · Traditional | 04/15/1994SE |
| K934271 | Beckman Synchron Lactate ReagentKHP · Traditional | 11/09/1993SE |
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Questions and answers
When was I.D.-Zone Immunofixation Electrophoresis Controls cleared by the FDA?
I.D.-Zone Immunofixation Electrophoresis Controls (K945522) received a 510(k) decision of Substantially Equivalent on December 12, 1994, 32 days after the submission was received.
What is the product code of K945522?
The FDA product code is DFT – Igm, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5550.