The following data is part of a premarket notification filed by Synermed, Inc. with the FDA for Creatinine-po Reagent Kit.
| Device ID | K943924 |
| 510k Number | K943924 |
| Device Name: | CREATININE-PO REAGENT KIT |
| Classification | Alkaline Picrate, Colorimetry, Creatinine |
| Applicant | SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Contact | Marcia J Artenz |
| Correspondent | Marcia J Artenz SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Product Code | CGX |
| CFR Regulation Number | 862.1225 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-12 |
| Decision Date | 1994-09-20 |