The following data is part of a premarket notification filed by Roche Diagnostics with the FDA for Elecsys Dhea-s Calcheck 5.
| Device ID | K103402 |
| 510k Number | K103402 |
| Device Name: | ELECSYS DHEA-S CALCHECK 5 |
| Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
| Applicant | Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250 |
| Contact | Kelly C O'maine Adams |
| Correspondent | Kelly C O'maine Adams Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250 |
| Product Code | JJX |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-11-19 |
| Decision Date | 2011-01-07 |
| Summary: | summary |