Cleared Traditional

K252440 - EasyTeleMed (2.0.2) (FDA 510(k) Clearance)

Oct 2025
Decision
59d
Days
Class 2
Risk

K252440 is an FDA 510(k) clearance for the EasyTeleMed (2.0.2). This device is classified as a Transmitters And Receivers, Physiological Signal, Radiofrequency (Class II - Special Controls, product code DRG).

Submitted by Ingeniars S.R.L. (Pisa, IT). The FDA issued a Cleared decision on October 2, 2025, 59 days after receiving the submission on August 4, 2025.

This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2910.

Submission Details

510(k) Number K252440 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 2025
Decision Date October 02, 2025
Days to Decision 59 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF

Device Classification

Product Code DRG - Transmitters And Receivers, Physiological Signal, Radiofrequency
Device Class Class II - Special Controls
CFR Regulation 21 CFR 870.2910