The following data is part of a premarket notification filed by Coopervision, Inc. with the FDA for Electric Instrument Table.
| Device ID | K832073 |
| 510k Number | K832073 |
| Device Name: | ELECTRIC INSTRUMENT TABLE |
| Classification | Stand, Instrument, Ac-powered, Ophthalmic |
| Applicant | COOPERVISION, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HMF |
| CFR Regulation Number | 886.1860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-28 |
| Decision Date | 1983-08-12 |