Aquilion Lightning, TSX-036A/1, V8.4
K-Number: K170019 · 2017-02-02
Device Summary
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. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K170019.
When did Aquilion Lightning, TSX-036A/1, V8.4 receive FDA 510(k) clearance?
Aquilion Lightning, TSX-036A/1, V8.4 received FDA 510(k) clearance on 2017-02-02, under 510(k) number K170019.
Who is the listed applicant for Aquilion Lightning, TSX-036A/1, V8.4?
The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Toshibamedical Systems Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JAK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.