510(k) K890622 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
SURG-E-TROL SYSTEM I AND SYSTEM II
| Applicant | Mentor O & O, Inc., Norwell MA, US |
| Decision | Substantially Equivalent, May 4, 1989 |
| Received | Feb 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890622
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.