The following data is part of a premarket notification filed by Dayton Mfg. Co. with the FDA for Summit Optics Contact Lens Remover.
| Device ID | K870072 |
| 510k Number | K870072 |
| Device Name: | SUMMIT OPTICS CONTACT LENS REMOVER |
| Classification | Inserter/remover Contact Lens |
| Applicant | DAYTON MFG. CO. P.O. BOX 271504 Tampa, FL 33624 |
| Contact | Michael P Dayton |
| Correspondent | Michael P Dayton DAYTON MFG. CO. P.O. BOX 271504 Tampa, FL 33624 |
| Product Code | KYE |
| CFR Regulation Number | 886.5420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-08 |
| Decision Date | 1987-02-12 |