The following data is part of a premarket notification filed by Dr. Bruno Lange Gmbh with the FDA for Photometer Lp 3.
| Device ID | K801563 |
| 510k Number | K801563 |
| Device Name: | PHOTOMETER LP 3 |
| Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
| Applicant | DR. BRUNO LANGE GMBH 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JJQ |
| CFR Regulation Number | 862.2300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-08 |
| Decision Date | 1980-08-20 |