510(k) K912877 ยท DQY Catheter, Percutaneous
PROFUSE INFUSION SYSTEM
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Sep 23, 1991 |
| Received | Jul 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912877
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.