510(k) K120120 ยท DQY Catheter, Percutaneous
AMPLATZER TORQVUE 45X45 DELIVERY SHEATH AMPLATZER TORQVUE LA1 DELIVERY SHEATH AMPLATZER TORQVUE LA2 SELIVERY SHEATH
| Applicant | Aga Medical Corporation, Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 15, 2012 |
| Received | Jan 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120120
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.