The following data is part of a premarket notification filed by Litton Medical Electronics with the FDA for Servomed Smc 108/111-426-24, 111-426.
| Device ID | K832022 |
| 510k Number | K832022 |
| Device Name: | SERVOMED SMC 108/111-426-24, 111-426 |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | LITTON MEDICAL ELECTRONICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-23 |
| Decision Date | 1983-11-16 |