The following data is part of a premarket notification filed by Bruce W. Martin O.d. And Edward Hensley with the FDA for Martin-hensley Segment Lens.
| Device ID | K897021 |
| 510k Number | K897021 |
| Device Name: | MARTIN-HENSLEY SEGMENT LENS |
| Classification | Lens, Contact (polymethylmethacrylate) |
| Applicant | BRUCE W. MARTIN O.D. AND EDWARD HENSLEY P.O. BOX 386 Gladwin, MI 48624 |
| Contact | Martin, Od |
| Correspondent | Martin, Od BRUCE W. MARTIN O.D. AND EDWARD HENSLEY P.O. BOX 386 Gladwin, MI 48624 |
| 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 | 1989-12-19 |
| Decision Date | 1990-06-22 |