The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for Spectronic 2000 Spectrophotometer.
| Device ID | K850767 |
| 510k Number | K850767 |
| Device Name: | SPECTRONIC 2000 SPECTROPHOTOMETER |
| Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
| 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 | JJQ |
| CFR Regulation Number | 862.2300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-02-25 |
| Decision Date | 1985-03-14 |