The following data is part of a premarket notification filed by Dmv Contact Lens Co. with the FDA for Contact Lens Remover And Inserter.
| Device ID | K780663 |
| 510k Number | K780663 |
| Device Name: | CONTACT LENS REMOVER AND INSERTER |
| Classification | Inserter/remover Contact Lens |
| Applicant | DMV CONTACT LENS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KYE |
| CFR Regulation Number | 886.5420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-20 |
| Decision Date | 1978-05-17 |