The following data is part of a premarket notification filed by Peter M. Tolliver with the FDA for La Vel Lateral View Extension Lens.
| Device ID | K820732 |
| 510k Number | K820732 |
| Device Name: | LA VEL LATERAL VIEW EXTENSION LENS |
| Classification | Spectacle, Magnifying |
| Applicant | PETER M. TOLLIVER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HOI |
| CFR Regulation Number | 886.5840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-17 |
| Decision Date | 1982-05-03 |