The following data is part of a premarket notification filed by Coopervision, Inc. with the FDA for Disposable Ocutome Probe.
| Device ID | K833371 |
| 510k Number | K833371 |
| Device Name: | DISPOSABLE OCUTOME PROBE |
| Classification | Instrument, Vitreous Aspiration And Cutting, Ac-powered |
| Applicant | COOPERVISION, INC. PERMALENS HOUSE 1 BOTLEY ROAD, HEDGE END Southampton, GB S033hb |
| Product Code | HQE |
| CFR Regulation Number | 886.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-27 |
| Decision Date | 1984-01-04 |