FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Ventilator, High Frequency
PMA: P850064
·
Supplement: S028
·
Decision Dec 17, 2015
Classifications
1
FEI Numbers
5
Registration Numbers
5
Basic Information
- Device Name
- Ventilator, High Frequency
- Trade Name
- LIFE PULSE HIGH FREQUENCY VENTILATOR, PATIENT BOX
- PMA Number
- P850064
- Supplement Number
- S028
- Device Class
- FDA Class 3
- Product Code
- LSZ
- Generic Name
- VENTILATOR, HIGH FREQUENCY
- Medical Specialty
- Unknown
- Advisory Committee
- Anesthesiology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 17, 2015
- Date Received
- February 4, 2015
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO UPGRADE THE LIFE PULSE HIGH LIFE PULSE HIGH FREQUENCY VENTILATOR 204 AND PATIENT BOX 213.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LSZ | Ventilator, High Frequency | FDA class 3 | Unknown |