The following data is part of a premarket notification filed by Jedmed Instrument Co. with the FDA for Reusable Surgical Keratoscope.
| Device ID | K864639 |
| 510k Number | K864639 |
| Device Name: | REUSABLE SURGICAL KERATOSCOPE |
| Classification | Keratoscope, Battery-powered |
| Applicant | JEDMED INSTRUMENT CO. 1430 HANLEY INDUSTRIAL CT. St. Louis, MO 63144 |
| Contact | Craig Rapp |
| Correspondent | Craig Rapp JEDMED INSTRUMENT CO. 1430 HANLEY INDUSTRIAL CT. St. Louis, MO 63144 |
| Product Code | HLR |
| CFR Regulation Number | 886.1350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-11-26 |
| Decision Date | 1986-12-29 |