The following data is part of a premarket notification filed by Robert E. Fenzl, M.d. with the FDA for Fenzl Reticle.
| Device ID | K801733 |
| 510k Number | K801733 |
| Device Name: | FENZL RETICLE |
| Classification | Spectacle, Magnifying |
| Applicant | ROBERT E. FENZL, M.D. 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 | 1980-07-25 |
| Decision Date | 1980-09-16 |