VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDING— 510(k) K131860
Substantially EquivalentUs Vascular, LLC
FDA 510(k) clearance K131860 for VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDING, Substantially Equivalent on 2013-09-27. Applicant: Us Vascular, LLC. Device class: 2.
Clearance details
- Applicant
- Us Vascular, LLC
- Product code
- Code JOP
- Device class
- Class 2
- Regulation
- 21 CFR 870.2880
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Recent devices under product code JOP
view allData sourced from openFDA. This site is unofficial and independent of the FDA.