The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Colorado Color Imaging Recorder.
| Device ID | K902230 |
| 510k Number | K902230 |
| Device Name: | COLORADO COLOR IMAGING RECORDER |
| Classification | Recorder, Paper Chart |
| Applicant | HONEYWELL, INC. P.O. BOX 5227 M.S. 219 Denver, CO 80217 |
| Contact | Carlos A Ortiz |
| Correspondent | Carlos A Ortiz HONEYWELL, INC. P.O. BOX 5227 M.S. 219 Denver, CO 80217 |
| Product Code | DSF |
| CFR Regulation Number | 870.2810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-05-17 |
| Decision Date | 1990-06-19 |