FlightPlan for Embolization
K-Number: K193261 · 2020-01-24
ApplicantGE Medical Systems SCS
Decision Date2020-01-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
FlightPlan for Embolization is a medical device manufactured by GE Medical Systems SCS. It received FDA 510(k) clearance on 2020-01-24 under approval number K193261. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FlightPlan for Embolization?
FlightPlan for Embolization is a medical device that received FDA 510(k) clearance on 2020-01-24. It is manufactured by GE Medical Systems SCS. The 510(k) number is K193261.
When was FlightPlan for Embolization approved by the FDA?
FlightPlan for Embolization received FDA 510(k) clearance on 2020-01-24, under approval number K193261.
What company makes FlightPlan for Embolization?
FlightPlan for Embolization is manufactured by GE Medical Systems SCS.
What is the FDA product code for FlightPlan for Embolization?
The FDA product code for FlightPlan for Embolization is LLZ.
Other Devices by GE Medical Systems SCS
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.