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FDA 510(k)

VMAT PRO

K-Number: K243488 · 2025-02-06

ApplicantTermosalud
Decision Date2025-02-06
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VMAT PRO is a medical device manufactured by Termosalud. It received FDA 510(k) clearance on 2025-02-06 under approval number K243488. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMAT PRO?

VMAT PRO is a medical device that received FDA 510(k) clearance on 2025-02-06. It is manufactured by Termosalud. The 510(k) number is K243488.

When was VMAT PRO approved by the FDA?

VMAT PRO received FDA 510(k) clearance on 2025-02-06, under approval number K243488.

What company makes VMAT PRO?

VMAT PRO is manufactured by Termosalud.

What is the FDA product code for VMAT PRO?

The FDA product code for VMAT PRO is ISA.

Other Devices by Termosalud

K230659Zionic Aesthetic K230412Symmed Elite Aesthetic K223680Eneka Pro K241656Eneka Selectif

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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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