The following data is part of a premarket notification filed by Ryder Intl. Corp. with the FDA for Opti-lens(tm) Contact Lens Case.
| Device ID | K915082 |
| 510k Number | K915082 |
| Device Name: | OPTI-LENS(TM) CONTACT LENS CASE |
| Classification | Case, Contact Lens |
| Applicant | RYDER INTL. CORP. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick, NJ 08902 |
| Contact | Patricia Bradstreet |
| Correspondent | Patricia Bradstreet RYDER INTL. CORP. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick, NJ 08902 |
| Product Code | LRX |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-12 |
| Decision Date | 1992-01-13 |