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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 the device name listed in this FDA 510(k) record. The listed applicant is Ingeniars S.R.L.. It received FDA 510(k) clearance on 2025-10-02 under 510(k) 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. The listed applicant is Ingeniars S.R.L.. The 510(k) number is K252440.

When did EasyTeleMed (2.0.2) receive FDA 510(k) clearance?

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

Who is the listed applicant for EasyTeleMed (2.0.2)?

The FDA 510(k) record lists Ingeniars S.R.L. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: DRG)

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.

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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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