510(k) K932619 ยท DQY Catheter, Percutaneous
TRANSSEPTAL INTRODUCER SET
| Applicant | Thomas Medical Products, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Aug 24, 1993 |
| Received | Jun 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932619
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.