510(k) K903625 ยท DPW Flowmeter, Blood, Cardiovascular
DOPPLER NEEDLE AND FLOW MONITOR
| Applicant | Peripheral Systems Group, Mountain View CA, US |
| Decision | Substantially Equivalent, Nov 7, 1990 |
| Received | Aug 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903625
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 22, 2010 | Escalon Medical Corp PD Access Vascular Access Device. Escalon Vascular Access, Inc., 2440 South 179th Street, New Berlin, WI 53146:
Model 78050 18 Gauge GA Doppler Guided Bare Needle Assembly, 2 3/4 in Length, 0.038 in g Terminated |
DPW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.