510(k) K100135 ยท DQY Catheter, Percutaneous
GDS-DC12
| Applicant | Guided Delivery Systems, Santa Clara CA, US |
| Decision | Substantially Equivalent, Apr 16, 2010 |
| Received | Jan 19, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100135
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.