The following data is part of a premarket notification filed by Roche Diagnostic Systems, Inc. with the FDA for Roche Calibrator Serum.
| Device ID | K942706 |
| 510k Number | K942706 |
| Device Name: | ROCHE CALIBRATOR SERUM |
| Classification | Calibrator, Multi-analyte Mixture |
| Applicant | ROCHE DIAGNOSTIC SYSTEMS, INC. 1080 U.S. HIGHWAY 202 Branchburg, NJ 08876 -3771 |
| Contact | Maria Feijoo |
| Correspondent | Maria Feijoo ROCHE DIAGNOSTIC SYSTEMS, INC. 1080 U.S. HIGHWAY 202 Branchburg, NJ 08876 -3771 |
| Product Code | JIX |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-08 |
| Decision Date | 1995-09-20 |