The following data is part of a premarket notification filed by Syva Co. with the FDA for Vista Thyroxine Uptake Assay.
| Device ID | K923676 |
| 510k Number | K923676 |
| Device Name: | VISTA THYROXINE UPTAKE ASSAY |
| Classification | Radioassay, Triiodothyronine Uptake |
| Applicant | SYVA CO. 3403 YERBA BUENA RD. San Jose, CA 95135 -1500 |
| Contact | Paul L Rogers |
| Correspondent | Paul L Rogers SYVA CO. 3403 YERBA BUENA RD. San Jose, CA 95135 -1500 |
| Product Code | KHQ |
| CFR Regulation Number | 862.1715 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-22 |
| Decision Date | 1992-10-09 |