The following data is part of a premarket notification filed by Keeler Instruments, Inc. with the FDA for Ophthalmic Scissors.
| Device ID | K811245 |
| 510k Number | K811245 |
| Device Name: | OPHTHALMIC SCISSORS |
| Classification | Scissors, Ophthalmic |
| Applicant | KEELER INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HNF |
| CFR Regulation Number | 886.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-04 |
| Decision Date | 1981-07-31 |