SENSILASE PAD-IQ— 510(k) K110438
Substantially EquivalentVasamed, Inc.
FDA 510(k) clearance K110438 for SENSILASE PAD-IQ, Substantially Equivalent on 2011-05-04. Applicant: Vasamed, Inc.. Device class: 2.
Clearance details
- Applicant
- Vasamed, Inc.
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Stoughton, WI, US
Recent devices under product code DPW
view allData sourced from openFDA. This site is unofficial and independent of the FDA.