510(k) K913517 ยท DQY Catheter, Percutaneous
ISOLATE INFUSION CATHETR SYSTEM
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Nov 5, 1991 |
| Received | Aug 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913517
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.