FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Permanent Defibrillator Electrodes
PMA: P020030
·
Supplement: S007
·
Decision Mar 15, 2012
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Permanent Defibrillator Electrodes
- Trade Name
- STELID II BTF/BJF STEROID COLLAR
- PMA Number
- P020030
- Supplement Number
- S007
- Device Class
- FDA Class 3
- Product Code
- NVY
- Generic Name
- Permanent defibrillator electrodes
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 15, 2012
- Date Received
- August 23, 2010
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR IMPROVING THE STEROID COLLAR MANUFACTURING PROCESS.
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 |
|---|---|---|---|
| NVY | Permanent Defibrillator Electrodes | FDA class 3 | Unknown |