The following data is part of a premarket notification filed by Oxford Medilog, Inc. with the FDA for Medilog 6000-fd Report Generator.
| Device ID | K890330 |
| 510k Number | K890330 |
| Device Name: | MEDILOG 6000-FD REPORT GENERATOR |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | OXFORD MEDILOG, INC. 11526 53RD. ST. N. Clearwater, FL 33520 |
| Contact | Michael J Smith |
| Correspondent | Michael J Smith OXFORD MEDILOG, INC. 11526 53RD. ST. N. Clearwater, FL 33520 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-23 |
| Decision Date | 1989-04-20 |