The following data is part of a premarket notification filed by Medicomp, Inc. with the FDA for Epi Cardia Sys. - Ambulatory Monitor.
| Device ID | K830013 |
| 510k Number | K830013 |
| Device Name: | EPI CARDIA SYS. - AMBULATORY MONITOR |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | MEDICOMP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-03 |
| Decision Date | 1983-02-28 |