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 |