510(k) K093195 ยท FCG Biopsy Needle
ECHOTIP ULTRA ENDOBRONCHIAL HIGH DEFINITION ULTASOUND NEEDLE, MODEL: ECHO-HD-22-EBUS-O
| Applicant | Cook Ireland, Ltd., Limerick, IE |
| Decision | Substantially Equivalent, Jan 21, 2010 |
| Received | Oct 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093195
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.