Lifepak 20 Defibrillator/ Monitor
FDA 510(k) K063119 · Medtronic Emergency Response Systems, Inc.
Submission
- Device name
- Lifepak 20 Defibrillator/ Monitor
- Applicant
- Medtronic Emergency Response Systems, Inc.
Redmond, WA, US - Received
- October 12, 2006
- Decision date
- December 22, 2006
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MKJ – Automated External Defibrillators (Non-Wearable)
- Device class
- Class III (high risk)
- Regulation
- 21 CFR 870.5310
- Specialty
- Cardiovascular
This device is a non-wearable prescription use only aed. These are devices that include automated external defibrillation. Automated external defibrillators use external pad-type electrodes to sense, detect, classify and treat (with an electrical shock) ventricular fibrillation. These devices are intended to be used on suspected victims of sudden cardiac arrest. A person in cardiac arrest is…
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More from Leonhard Lang GmbH
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Questions and answers
When was Lifepak 20 Defibrillator/ Monitor cleared by the FDA?
Lifepak 20 Defibrillator/ Monitor (K063119) received a 510(k) decision of Substantially Equivalent on December 22, 2006, 71 days after the submission was received.
What is the product code of K063119?
The FDA product code is MKJ – Automated External Defibrillators (Non-Wearable), a Class III (high risk) device regulated under 21 CFR 870.5310.