The following data is part of a premarket notification filed by Cadwell Laboratories, Inc. with the FDA for Contrast Sensitivity Equipment.
| Device ID | K830770 |
| 510k Number | K830770 |
| Device Name: | CONTRAST SENSITIVITY EQUIPMENT |
| Classification | Photostimulator, Ac-powered |
| Applicant | CADWELL LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HLX |
| CFR Regulation Number | 886.1630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-03-11 |
| Decision Date | 1983-04-28 |