510(k) K070357 ยท DRA Catheter, Steerable
FLEXCATH STEERABLE SHEATH & DILATOR
| Applicant | Cryocath Technologies, Inc., Santa Fe NM, US |
| Decision | Substantially Equivalent, Dec 28, 2007 |
| Received | Feb 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070357
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.