The following data is part of a premarket notification filed by Cadwell Laboratories, Inc. with the FDA for Gold Foil Erg Electrodes.
| Device ID | K820254 |
| 510k Number | K820254 |
| Device Name: | GOLD FOIL ERG ELECTRODES |
| Classification | Electrode, Corneal |
| Applicant | CADWELL LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HLZ |
| CFR Regulation Number | 886.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-02-01 |
| Decision Date | 1982-04-09 |