510(k) K152202 ยท DQY Catheter, Percutaneous
Intermediate Catheter, 105 cm, Intermediate Catheter, 115cm, Intermediate Catheter , 125cm
| Applicant | Tni Manufacturing, Inc., Sunrise FL, US |
| Decision | Substantially Equivalent, Dec 14, 2015 |
| Received | Aug 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152202
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.