The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Vc 430 Video Converter.
| Device ID | K810164 |
| 510k Number | K810164 |
| Device Name: | VC 430 VIDEO CONVERTER |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | HONEYWELL, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-01-22 |
| Decision Date | 1981-02-25 |