FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Nitric Oxide Generator And Delivery System
PMA: P200044
·
Supplement: S003
·
Decision Sep 10, 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
- S003
- 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
- September 10, 2023
- Date Received
- May 1, 2023
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for minor software changes to add support for future language translations, enhance manfucaturability and serviceability, refine alarms, limit the range for date changes, and for preparation of future compatibility and enhancements.
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 |