510(k) K051247 ยท FCG Biopsy Needle
SONOTIP II ULTRASOUND NEEDLE SYSTEM
| Applicant | Medi-Globe Corp., Tempe AZ, US |
| Decision | Substantially Equivalent, Jun 16, 2005 |
| Received | May 16, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051247
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.