The following data is part of a premarket notification filed by Oxford Medilog, Inc. with the FDA for Oxford Vdt-40 Display Terminal.
Device ID | K852207 |
510k Number | K852207 |
Device Name: | OXFORD VDT-40 DISPLAY TERMINAL |
Classification | Detector And Alarm, Arrhythmia |
Applicant | OXFORD MEDILOG, INC. 11526 53RD. ST. N. Clearwater, FL 33520 |
Contact | John K Laurie |
Correspondent | John K Laurie 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 | 1985-05-21 |
Decision Date | 1985-06-11 |