The following data is part of a premarket notification filed by Synermed, Inc. with the FDA for Synermed Magnesium Reagent Kit.
| Device ID | K902919 |
| 510k Number | K902919 |
| Device Name: | SYNERMED MAGNESIUM REAGENT KIT |
| Classification | Photometric Method, Magnesium |
| 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 | JGJ |
| CFR Regulation Number | 862.1495 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-07-03 |
| Decision Date | 1990-07-31 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05060500091927 | K902919 | 000 |
| 05060500091200 | K902919 | 000 |
| 05060500091194 | K902919 | 000 |
| 05060500091187 | K902919 | 000 |
| 05060500091170 | K902919 | 000 |
| 05060500091163 | K902919 | 000 |