The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for Projector, Accu-chart Acuity.
| Device ID | K781658 |
| 510k Number | K781658 |
| Device Name: | PROJECTOR, ACCU-CHART ACUITY |
| Classification | Projector, Ophthalmic |
| Applicant | BAUSCH & LOMB, INC. 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 | 1978-09-28 |
| Decision Date | 1978-10-17 |