The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for Bausch & Lomb Accu-chart 3 Acuity Projector.
| Device ID | K862519 |
| 510k Number | K862519 |
| Device Name: | BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR |
| Classification | Projector, Ophthalmic |
| Applicant | BAUSCH & LOMB, INC. 1400 NORTH GOODMAN ST. P.O.BOX 450 Rochester, NY 14692 |
| Contact | Nicholas A Walp |
| Correspondent | Nicholas A Walp BAUSCH & LOMB, INC. 1400 NORTH GOODMAN ST. P.O.BOX 450 Rochester, NY 14692 |
| Product Code | HOS |
| CFR Regulation Number | 886.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-07-01 |
| Decision Date | 1986-07-23 |