The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Dual Trace Patient Monitor 116,118,120.
| Device ID | K810179 |
| 510k Number | K810179 |
| Device Name: | DUAL TRACE PATIENT MONITOR 116,118,120 |
| Classification | Computer, Blood-pressure |
| Applicant | HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSK |
| CFR Regulation Number | 870.1110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-01-22 |
| Decision Date | 1981-02-25 |