Home › Device types › DAK
Complement C1q, Antigen, Antiserum, Control
FDA product code DAK · Class 2 · Immunology
9
Registered devices
0
Adverse events
3
Recalls
28
510(k) clearances
Devices with this code
CIC-C1q ELISA Kit — Bühlmann Laboratories AGAntiserum to Human C1q — KENT LABORATORIES INCHuman Complement C1q BINDARID™ Radial Immunodiffusion Kit — THE BINDING SITE GROUP LIMITEDScanlisa C1q Elisa 96 Test — SCIMEDX CORPORATIONAnti Human Complement C1q FITC — KENT LABORATORIES INCQUANTA Lite® C1q CIC ELISA — INOVA DIAGNOSTICS, INC.MicroVue — QUIDEL CORPORATIONMicroVue — QUIDEL CORPORATIONC1q Plates & Calibrator Sets — SCIMEDX CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-04-04 | Diagnostic Hybrids, Inc. | There is a potential for the slope of the standard curve to fail to meet the assay validation requirements for the assay. |
| 2015-11-03 | Diagnostic Hybrids, Inc. | A component of the kit was found to contain bacterial contamination. |
| 2009-10-28 | Inova Diagnostics Incorporated | The recall was initiated after the binding site notified Inova Diagnostics, inc. that the affected Bindazyme Human C1q binding Circulating Immune Complex EIA Ki |
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