The following data is part of a premarket notification filed by Synermed, Inc. with the FDA for Synermedir Cal I And Synermed Ir Cal Ii.
| Device ID | K940571 |
| 510k Number | K940571 |
| Device Name: | SYNERMEDIR CAL I AND SYNERMED IR CAL II |
| Classification | Calibrator, Multi-analyte Mixture |
| Applicant | SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Contact | Marcia J Arentz |
| Correspondent | Marcia J Arentz SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Product Code | JIX |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-08 |
| Decision Date | 1994-04-21 |