The following data is part of a premarket notification filed by Magnivision, Inc. with the FDA for Item #352/#cs352* Contact Lens Cases.
| Device ID | K890533 |
| 510k Number | K890533 |
| Device Name: | ITEM #352/#CS352* CONTACT LENS CASES |
| Classification | Case, Contact Lens |
| Applicant | MAGNIVISION, INC. P.O. BOX 817 Miami, FL 33152 |
| Contact | Roy Hirschfeld |
| Correspondent | Roy Hirschfeld MAGNIVISION, INC. P.O. BOX 817 Miami, FL 33152 |
| Product Code | LRX |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-02-02 |
| Decision Date | 1989-06-23 |