The following data is part of a premarket notification filed by Cilco, Inc. with the FDA for Cilcor Ophthalmic Instruments.
| Device ID | K843992 |
| 510k Number | K843992 |
| Device Name: | CILCOR OPHTHALMIC INSTRUMENTS |
| Classification | Forceps, Ophthalmic |
| Applicant | CILCO, INC. 1616 13TH. AVE. SUITE 200 Huntington, WV 25701 |
| Contact | Rick Mccarley |
| Correspondent | Rick Mccarley CILCO, INC. 1616 13TH. AVE. SUITE 200 Huntington, WV 25701 |
| Product Code | HNR |
| CFR Regulation Number | 886.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-11 |
| Decision Date | 1984-11-21 |