ViewPoint 6
K-Number: K192917 · 2020-01-06
ApplicantGe Medical Systems Ultrasound And
Decision Date2020-01-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ViewPoint 6 is a medical device manufactured by Ge Medical Systems Ultrasound And. It received FDA 510(k) clearance on 2020-01-06 under approval number K192917. 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 ViewPoint 6?
ViewPoint 6 is a medical device that received FDA 510(k) clearance on 2020-01-06. It is manufactured by Ge Medical Systems Ultrasound And. The 510(k) number is K192917.
When was ViewPoint 6 approved by the FDA?
ViewPoint 6 received FDA 510(k) clearance on 2020-01-06, under approval number K192917.
What company makes ViewPoint 6?
ViewPoint 6 is manufactured by Ge Medical Systems Ultrasound And.
What is the FDA product code for ViewPoint 6?
The FDA product code for ViewPoint 6 is LLZ.
Other Devices by Ge Medical Systems Ultrasound And
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.