510(k) K071883 ยท GEX Powered Laser Surgical Instrument
IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2
| Applicant | Cyden Limited, Swansea, Wales, GB |
| Decision | Substantially Equivalent, Jan 23, 2008 |
| Received | Jul 9, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071883
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.