The following data is part of a premarket notification filed by Maurry Biological Co. with the FDA for All-in-one Hard Contact Lens Solution.
| Device ID | K853807 |
| 510k Number | K853807 |
| Device Name: | ALL-IN-ONE HARD CONTACT LENS SOLUTION |
| Classification | Lens, Contact (polymethylmethacrylate) |
| Applicant | MAURRY BIOLOGICAL CO. 6109 SOUTH WESTERN AVE. Los Angeles, CA 90047 |
| Contact | Des Rochers |
| Correspondent | Des Rochers MAURRY BIOLOGICAL CO. 6109 SOUTH WESTERN AVE. Los Angeles, CA 90047 |
| Product Code | HPX |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-11 |
| Decision Date | 1985-12-16 |