The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Ls-8 Visicorder.
| Device ID | K790825 |
| 510k Number | K790825 |
| Device Name: | LS-8 VISICORDER |
| Classification | Recorder, Paper Chart |
| Applicant | HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSF |
| CFR Regulation Number | 870.2810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-30 |
| Decision Date | 1979-05-31 |