510(k) K973485 ยท FQH Lavage, Jet
CLEARVIEW BLOWER/MISTER
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Dec 8, 1997 |
| Received | Sep 15, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973485
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 10, 2024 | Medtronic Perfusion Systems Medtronic Clearview Blower/Mister, Model Number 22120 Open, Classified |
FQH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.