The following data is part of a premarket notification filed by Surgidev Corp. with the FDA for Karickhoff Keratoscope.
| Device ID | K830008 |
| 510k Number | K830008 |
| Device Name: | KARICKHOFF KERATOSCOPE |
| Classification | Keratoscope, Battery-powered |
| Applicant | SURGIDEV CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HLR |
| CFR Regulation Number | 886.1350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-03 |
| Decision Date | 1983-01-26 |