510(k) K070129 ยท FCG Biopsy Needle
SONOTIP II ULTRASOUND NEEDLE SYSTEM
| Applicant | Medi-Globe Corporation, Tempe AZ, US |
| Decision | Substantially Equivalent, Jan 31, 2007 |
| Received | Jan 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070129
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.