CORPATH 200 SYSTEM— 510(k) K120834
Substantially EquivalentCorindus, Inc.
FDA 510(k) clearance K120834 for CORPATH 200 SYSTEM, Substantially Equivalent on 2012-07-19. 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
- Baltimore, MD, US
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