The following data is part of a premarket notification filed by J.t. Baker Chemical Co. with the FDA for Baker Diagnostic Ultra-rate Sodium/pot..
| Device ID | K801795 |
| 510k Number | K801795 |
| Device Name: | BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT. |
| Classification | Electrode, Ion Specific, Sodium |
| Applicant | J.T. BAKER CHEMICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JGS |
| CFR Regulation Number | 862.1665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-29 |
| Decision Date | 1980-09-16 |