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FDA 510(k)

EasyTeleMed (2.0.2)

K-Number: K252440 · 2025-10-02

ApplicantIngeniars S.R.L.
Decision Date2025-10-02
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EasyTeleMed (2.0.2) is a medical device manufactured by Ingeniars S.R.L.. It received FDA 510(k) clearance on 2025-10-02 under approval number K252440. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EasyTeleMed (2.0.2)?

EasyTeleMed (2.0.2) is a medical device that received FDA 510(k) clearance on 2025-10-02. It is manufactured by Ingeniars S.R.L.. The 510(k) number is K252440.

When was EasyTeleMed (2.0.2) approved by the FDA?

EasyTeleMed (2.0.2) received FDA 510(k) clearance on 2025-10-02, under approval number K252440.

What company makes EasyTeleMed (2.0.2)?

EasyTeleMed (2.0.2) is manufactured by Ingeniars S.R.L..

What is the FDA product code for EasyTeleMed (2.0.2)?

The FDA product code for EasyTeleMed (2.0.2) is DRG.

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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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