CardIQ Flow— 510(k) K192277
Substantially EquivalentGE Medical Systems SCS
FDA 510(k) clearance K192277 for CardIQ Flow, Substantially Equivalent on 2020-02-14. Applicant: GE Medical Systems SCS. Device class: 2.
Clearance details
- Applicant
- GE Medical Systems SCS
- Product code
- Code KPS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1200
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buc, FR
Recent devices under product code KPS
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