510(k) K100184 ยท DQY Catheter, Percutaneous
FUSTAR STEERABLE INTRODUCERS
| Applicant | Lifetech Scientific (Shenzhen) Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Feb 14, 2011 |
| Received | Jan 21, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100184
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.