510(k) K102385 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
NORFOLK MEDICAL NORPORT FAMILY OF PORTS
| Applicant | Norfolk Medical Products, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Jan 14, 2011 |
| Received | Aug 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102385
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.