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FDA 510(k)

VisAble.IO

K-Number: K240773 · 2024-04-15

ApplicantTechsomed
Decision Date2024-04-15
Product CodeQTZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VisAble.IO is a medical device manufactured by Techsomed. It received FDA 510(k) clearance on 2024-04-15 under approval number K240773. The device is classified under product code QTZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VisAble.IO?

VisAble.IO is a medical device that received FDA 510(k) clearance on 2024-04-15. It is manufactured by Techsomed. The 510(k) number is K240773.

When was VisAble.IO approved by the FDA?

VisAble.IO received FDA 510(k) clearance on 2024-04-15, under approval number K240773.

What company makes VisAble.IO?

VisAble.IO is manufactured by Techsomed.

What is the FDA product code for VisAble.IO?

The FDA product code for VisAble.IO is QTZ.

Other Devices by Techsomed

K223639VisAble.IO

Related Devices (Code: QTZ)

K220256MIM-AblationMim Software, Inc. K222222Artemis, Artemis TPO, Artemis MXEigen K222938Ablation-fitR.A.W. S.R.L K223639VisAble.IOTechsomed K240796myAblation Guide (VB80A)Siemens Healthcare GmbH K251931BioTraceIO Vision (V1.7)Techsomed Medical Technologies

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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