The following data is part of a premarket notification filed by Roche Diagnostics with the FDA for Elecsys Folate Iii.
| Device ID | K141426 |
| 510k Number | K141426 |
| Device Name: | ELECSYS FOLATE III |
| Classification | Acid, Folic, Radioimmunoassay |
| Applicant | Roche Diagnostics 9115 HAGUE ROAD Indianapolis, IN 46250 -0416 |
| Contact | Kelli Turner |
| Correspondent | Kelli Turner Roche Diagnostics 9115 HAGUE ROAD Indianapolis, IN 46250 -0416 |
| Product Code | CGN |
| CFR Regulation Number | 862.1295 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-05-30 |
| Decision Date | 2014-10-17 |
| Summary: | summary |