The following data is part of a premarket notification filed by Orbtek, Inc. with the FDA for Orbscan(tm) Keratometer.
| Device ID | K940647 |
| 510k Number | K940647 |
| Device Name: | ORBSCAN(TM) KERATOMETER |
| Classification | Keratoscope, Ac-powered |
| Applicant | ORBTEK, INC. 3030 SOUTH MAIN ST. SUITE 600 Salt Lake City, UT 84115 |
| Contact | Robert P Byard |
| Correspondent | Robert P Byard ORBTEK, INC. 3030 SOUTH MAIN ST. SUITE 600 Salt Lake City, UT 84115 |
| Product Code | HLQ |
| CFR Regulation Number | 886.1350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-15 |
| Decision Date | 1994-07-06 |