Modular Telemetry System for the Vision Telepak, Model 20701

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K043354 ↗

FDA Product Code

DRT

Device Class

Class II

Regulation

21 CFR Part 870.2300

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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See all devices from Invivo Research, Inc. →