The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for 902 Na/k.
| Device ID | K811896 |
| 510k Number | K811896 |
| Device Name: | 902 NA/K |
| Classification | Electrode, Ion Specific, Sodium |
| Applicant | CORNING MEDICAL & SCIENTIFIC 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 | 1981-07-01 |
| Decision Date | 1981-07-23 |