The following data is part of a premarket notification filed by Marquette Electronics, Inc. with the FDA for Three Channel Monitor Series 6700.
| Device ID | K830899 |
| 510k Number | K830899 |
| Device Name: | THREE CHANNEL MONITOR SERIES 6700 |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | MARQUETTE ELECTRONICS, INC. 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 | 1983-03-21 |
| Decision Date | 1983-04-12 |