CorPath GRX System— 510(k) K160121
Substantially EquivalentCorindus, Inc.
FDA 510(k) clearance K160121 for CorPath GRX System, Substantially Equivalent on 2016-10-27. Applicant: Corindus, Inc.. Device class: 2.
Clearance details
- Applicant
- Corindus, Inc.
- Product code
- Code DXX
- Device class
- Class 2
- Regulation
- 21 CFR 870.1290
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Waltham, MA, US
Recent devices under product code DXX
view allMore clearances from Corindus, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.