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FDA 510(k)

Aquilion Serve (TSX-307A/1) V1.3

K-Number: K231281 · 2023-09-19

ApplicantCanon Medical Systems Corporation
Decision Date2023-09-19
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Aquilion Serve (TSX-307A/1) V1.3 is a medical device manufactured by Canon Medical Systems Corporation. It received FDA 510(k) clearance on 2023-09-19 under approval number K231281. 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 Serve (TSX-307A/1) V1.3?

Aquilion Serve (TSX-307A/1) V1.3 is a medical device that received FDA 510(k) clearance on 2023-09-19. It is manufactured by Canon Medical Systems Corporation. The 510(k) number is K231281.

When was Aquilion Serve (TSX-307A/1) V1.3 approved by the FDA?

Aquilion Serve (TSX-307A/1) V1.3 received FDA 510(k) clearance on 2023-09-19, under approval number K231281.

What company makes Aquilion Serve (TSX-307A/1) V1.3?

Aquilion Serve (TSX-307A/1) V1.3 is manufactured by Canon Medical Systems Corporation.

What is the FDA product code for Aquilion Serve (TSX-307A/1) V1.3?

The FDA product code for Aquilion Serve (TSX-307A/1) V1.3 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.

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