510(k) K990220 ยท FCG Biopsy Needle
MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM
| Applicant | Medi-Globe Corp., Tempe AZ, US |
| Decision | Substantially Equivalent, Mar 31, 1999 |
| Received | Jan 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990220
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.