The following data is part of a premarket notification filed by Richmond Products, Inc. with the FDA for Confirmation Tests.
| Device ID | K873907 |
| 510k Number | K873907 |
| Device Name: | CONFIRMATION TESTS |
| Classification | Set, Lens, Trial, Ophthalmic |
| Applicant | RICHMOND PRODUCTS, INC. 1021 SO ROGERS CIRCLE Boca Raton, FL 33487 -2894 |
| Contact | Lloyd Powell |
| Correspondent | Lloyd Powell RICHMOND PRODUCTS, INC. 1021 SO ROGERS CIRCLE Boca Raton, FL 33487 -2894 |
| Product Code | HPC |
| CFR Regulation Number | 886.1405 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-09-25 |
| Decision Date | 1987-12-29 |