The following data is part of a premarket notification filed by Advantage Medical Systems, Inc. with the FDA for Central Display System #cs400.
| Device ID | K821479 |
| 510k Number | K821479 |
| Device Name: | CENTRAL DISPLAY SYSTEM #CS400 |
| Classification | System, Monitoring, Perinatal |
| Applicant | ADVANTAGE MEDICAL SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HGM |
| CFR Regulation Number | 884.2740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-18 |
| Decision Date | 1982-06-25 |