Aquilion Lightning, TSX-036A/1, V8.4
K-Number: K170019 · 2017-02-02
ApplicantToshibamedical Systems Corporation
Decision Date2017-02-02
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Aquilion Lightning, TSX-036A/1, V8.4 is a medical device manufactured by Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-02-02 under approval number K170019. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aquilion Lightning, TSX-036A/1, V8.4?
Aquilion Lightning, TSX-036A/1, V8.4 is a medical device that received FDA 510(k) clearance on 2017-02-02. It is manufactured by Toshibamedical Systems Corporation. The 510(k) number is K170019.
When was Aquilion Lightning, TSX-036A/1, V8.4 approved by the FDA?
Aquilion Lightning, TSX-036A/1, V8.4 received FDA 510(k) clearance on 2017-02-02, under approval number K170019.
What company makes Aquilion Lightning, TSX-036A/1, V8.4?
Aquilion Lightning, TSX-036A/1, V8.4 is manufactured by Toshibamedical Systems Corporation.
What is the FDA product code for Aquilion Lightning, TSX-036A/1, V8.4?
The FDA product code for Aquilion Lightning, TSX-036A/1, V8.4 is JAK.
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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.