The following data is part of a premarket notification filed by Mosebach Electric & Supply with the FDA for Miller/nadler Glare Tester.
| Device ID | K812706 |
| 510k Number | K812706 |
| Device Name: | MILLER/NADLER GLARE TESTER |
| Classification | Projector, Ophthalmic |
| Applicant | MOSEBACH ELECTRIC & SUPPLY 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 | 1981-09-24 |
| Decision Date | 1981-11-16 |