The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for B & L Ophthalmic Chair.
| Device ID | K791105 |
| 510k Number | K791105 |
| Device Name: | B & L OPHTHALMIC CHAIR |
| Classification | Stand, Instrument, Ac-powered, Ophthalmic |
| Applicant | BAUSCH & LOMB, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HMF |
| CFR Regulation Number | 886.1860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-06-13 |
| Decision Date | 1979-07-24 |