Argos— 510(k) K181372
Substantially EquivalentRetia Medical, LLC
FDA 510(k) clearance K181372 for Argos, Substantially Equivalent on 2018-12-13. Applicant: Retia Medical, LLC. Device class: 2.
Clearance details
- Applicant
- Retia Medical, LLC
- Product code
- Code DXG
- Device class
- Class 2
- Regulation
- 21 CFR 870.1435
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Valhalla, NY, US
Recent devices under product code DXG
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