Arrhythmia Technologies, Inc.

Arrhythmia Technologies, Inc. holds 2 FDA 510(k) medical device clearances, cleared in 1992.

Top product codes for Arrhythmia Technologies, Inc.

DRF — Cardiovascular2 devices

Recent clearances by Arrhythmia Technologies, Inc.

K915563 — DIAGNOSTIC EP CATHETERCode DRF·1992-03-09
K915640 — VOYAGR SERIES OF DEFLECTABLE DIAGOSTIC EP CATHETERCode DRF·1992-03-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.