Home › Device types › KRE

Analyzer, Pacemaker Generator Function, Indirect

FDA product code KRE · Class 2 · Cardiovascular

22

Registered devices

43

Adverse events

0

Recalls

13

510(k) clearances

Devices with this code

PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART OPTIMA™ System — MEDTRONIC, INC.NA — MEDTRONIC, INC.PACEART® SYSTEM ECG MODULE — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART OPTIMA™ SYSTEM — MEDTRONIC, INC.PACEART OPTIMA™ System — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.Paceart Optima™ System 1.6 with Analytics — MEDTRONIC, INC.PACEART OPTIMA™ SYSTEM — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART OPTIMA™ SYSTEM — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III, CardioVoice® TTM Assistant Software — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART OPTIMA™ SYSTEM — MEDTRONIC, INC.PACEART OPTIMA™ System — MEDTRONIC, INC.PACEART® SYSTEM GET CONNECTED III — MEDTRONIC, INC.PACEART OPTIMA™ System — MEDTRONIC, INC.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.