VASCULIZER— 510(k) K791418
Substantially EquivalentDiagnostics Intl.
FDA 510(k) clearance K791418 for VASCULIZER, Substantially Equivalent on 1979-10-04. Applicant: Diagnostics Intl.. Device class: 2.
Clearance details
- Applicant
- Diagnostics Intl.
- Product code
- Product code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code DPW
view all- K261714 — FlowXL® System: FlowXL Flowmeter and compatible Flowprobes and Flowsensors
- K260700 — BlueDop Vascular Expert
- K252810 — FloPatch FP120
- K251904 — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01) +1 more
- K251114 — FloPatch FP120
Data sourced from openFDA. This site is unofficial and independent of the FDA.