LIFENET SYSTEM— 510(k) K102757
Substantially EquivalentPhysio-Control, Inc.
FDA 510(k) clearance K102757 for LIFENET SYSTEM, Substantially Equivalent on 2010-11-05. Applicant: Physio-Control, Inc.. Device class: 2.
Clearance details
- Applicant
- Physio-Control, Inc.
- Product code
- Code MSX
- Device class
- Class 2
- Regulation
- 21 CFR 870.2300
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Redmond, WA, US
Recent devices under product code MSX
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view all- K253099 — LIFEPAK 15 AC Power Adapter (41577-000333)
- K240156 — LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021) +1 more
- K182503 — Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors
- K142430 — LIFEPAK 15 monitor/defibrillator
- K130454 — LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR
Adverse events under product code MSX
product code MSX- Death
- 59
- Total
- 59
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.