510(k) K123842 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
LAWMAX DILATOR
| Applicant | Lifetech Scientific (Shenzhen) Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 24, 2013 |
| Received | Dec 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123842
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.