The following data is part of a premarket notification filed by Techna Vision with the FDA for Techna Vision, Inc.electric Table.
| Device ID | K853744 |
| 510k Number | K853744 |
| Device Name: | TECHNA VISION, INC.ELECTRIC TABLE |
| Classification | Table, Instrument, Powered, Ophthalmic |
| Applicant | TECHNA VISION 11489 WOODSIDE AVE. Santee, CA 92071 |
| Contact | James T Kelley |
| Correspondent | James T Kelley TECHNA VISION 11489 WOODSIDE AVE. Santee, CA 92071 |
| Product Code | HRJ |
| CFR Regulation Number | 886.4855 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-06 |
| Decision Date | 1985-10-17 |