FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Nitric Oxide Generator And Delivery System
PMA: P200044
·
Supplement: S002
·
Decision Apr 21, 2023
Classifications
1
FEI Numbers
3
Registration Numbers
3
Basic Information
- Device Name
- Nitric Oxide Generator And Delivery System
- Trade Name
- LungFit PH
- PMA Number
- P200044
- Supplement Number
- S002
- Device Class
- FDA Class 3
- Product Code
- QTB
- Generic Name
- Nitric Oxide Generator and Delivery System
- Medical Specialty
- Unknown
- Advisory Committee
- Anesthesiology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- April 21, 2023
- Date Received
- March 24, 2023
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for an update to Pre-Use Guide (20092-01) to include a figure for bagging system connections which is already included in the Operators Manual and included in training.
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 |
|---|---|---|---|
| QTB | Nitric Oxide Generator And Delivery System | FDA class 3 | Unknown |