The following data is part of a premarket notification filed by Syva Co. with the FDA for Vista Folate Assay.
| Device ID | K934121 |
| 510k Number | K934121 |
| Device Name: | VISTA FOLATE ASSAY |
| Classification | Acid, Folic, Radioimmunoassay |
| Applicant | SYVA CO. 3403 YERBA BUENA RD. P.O. BOX 49013 San Jose, CA 95161 -9013 |
| Contact | Paul Rogers |
| Correspondent | Paul Rogers SYVA CO. 3403 YERBA BUENA RD. P.O. BOX 49013 San Jose, CA 95161 -9013 |
| Product Code | CGN |
| CFR Regulation Number | 862.1295 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-08-25 |
| Decision Date | 1993-10-22 |