The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Scanning Sys., Auto. Comp., Acs1000.
| Device ID | K772140 |
| 510k Number | K772140 |
| Device Name: | SCANNING SYS., AUTO. COMP., ACS1000 |
| Classification | Device, Automated Cell-locating |
| Applicant | HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JOY |
| CFR Regulation Number | 864.5260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-11-14 |
| Decision Date | 1977-12-05 |