510(k) K994229 ยท DQY Catheter, Percutaneous
VERIPATH PERIPHERAL GUIDING CATHETER
| Applicant | Advanced Cardiovascular Systems, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, Feb 25, 2000 |
| Received | Dec 16, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K994229
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.