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Tester, Pacemaker Electrode Function
FDA product code DTA · Class 2 · Cardiovascular
8
Registered devices
9
Adverse events
2
Recalls
10
510(k) clearances
Devices with this code
CareLink SmartSync™ — MEDTRONIC, INC.CareLink SmartSync™ — MEDTRONIC, INC.CareLink SmartSync™ Common Application — MEDTRONIC, INC.CareLink SmartSync™ — MEDTRONIC, INC.CareLink SmartSync™ Azure Astra Application — MEDTRONIC, INC.CareLink SmartSync™ — MEDTRONIC, INC.CareLink SmartSync™ Common Application — MEDTRONIC, INC.Osypka Medical — Osypka Medical GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-08-31 | Remington Medical Inc. | The vector selector has an electrical design flaw which prevents RV pacing. |
| 2004-10-20 | Medtronic Inc. Cardiac Rhythm Managment | A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length. |
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