The following data is part of a premarket notification filed by Crestat Diagnostics, Inc. with the FDA for N-assay Tia Transferrin Test Kit.
| Device ID | K964295 |
| 510k Number | K964295 |
| Device Name: | N-ASSAY TIA TRANSFERRIN TEST KIT |
| Classification | Transferrin, Antigen, Antiserum, Control |
| Applicant | CRESTAT DIAGNOSTICS, INC. 25549 ADAMS AVE. Murrieta, CA 92562 |
| Product Code | DDG |
| CFR Regulation Number | 866.5880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-10-29 |
| Decision Date | 1997-06-16 |