The following data is part of a premarket notification filed by American Optical Corp. with the FDA for Ultramatic Project-o-chart Ophth. Proj.
| Device ID | K811180 |
| 510k Number | K811180 |
| Device Name: | ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ |
| Classification | Projector, Ophthalmic |
| Applicant | AMERICAN OPTICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HOS |
| CFR Regulation Number | 886.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-28 |
| Decision Date | 1981-05-15 |