The following data is part of a premarket notification filed by Bausch & Lomb Incorporated with the FDA for Rigid Gas Permeable Contact Lens.
| Device ID | K013762 |
| 510k Number | K013762 |
| Device Name: | RIGID GAS PERMEABLE CONTACT LENS |
| Classification | Lens, Contact (other Material) - Daily |
| Applicant | BAUSCH & LOMB INCORPORATED 1400 N. GOODMAN ST. PO BOX 30450 Rochester, NY 14603 -0450 |
| Contact | Debra L.b. Ketchum |
| Correspondent | Debra L.b. Ketchum BAUSCH & LOMB INCORPORATED 1400 N. GOODMAN ST. PO BOX 30450 Rochester, NY 14603 -0450 |
| Product Code | HQD |
| CFR Regulation Number | 886.5916 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-11-13 |
| Decision Date | 2002-04-03 |
| Summary: | summary |