510(k) K954816 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
STORZ DP4800 DELUXE , STORZ DP4801 BASIC W/REFLUX, DP4801 BASIC POSTERIOR VITRECTOMY PACK WITH VARIABLE PORT CUTTER & RX
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 4, 1996 |
| Received | Oct 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954816
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.