FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Sealant, Polymerizing
PMA: P010047
·
Supplement: S002
·
Decision Apr 15, 2010
Classifications
1
FEI Numbers
15
Registration Numbers
15
Basic Information
- Device Name
- Sealant, Polymerizing
- Trade Name
- NEOMEND PROGEL PLEURAL AIR LEAK SEALANT
- PMA Number
- P010047
- Supplement Number
- S002
- Device Class
- FDA Class 3
- Product Code
- NBE
- Generic Name
- Sealant, polymerizing
- Medical Specialty
- Unknown
- Advisory Committee
- Anesthesiology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- April 15, 2010
- Date Received
- March 16, 2010
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
CHANGE FROM A MANUAL MANUFACTURING PROCESS TO AUTOMATED PROCESS FOR FILLING A COMPONENT.
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 |
|---|---|---|---|
| NBE | Sealant, Polymerizing | FDA class 3 | Unknown |