510(k) K063333 ยท FSY Light, Surgical, Ceiling Mounted
M3
| Applicant | Mavig GmbH, Munchen, DE |
| Decision | Substantially Equivalent, Nov 21, 2006 |
| Received | Nov 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063333
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 12, 2012 | Siemens Medical Solutions USA, Inc MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system
Ceiling mounted surgical light Terminated |
FSY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.