FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Permanent Pacemaker Electrode
PMA: P830061
·
Supplement: S001
·
Decision Sep 25, 1986
Classifications
1
FEI Numbers
24
Registration Numbers
24
Basic Information
- Device Name
- Permanent Pacemaker Electrode
- Trade Name
- STEROID TIP(TM) MODEL 4503&4003 TRANSVENOUS PACING
- PMA Number
- P830061
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- DTB
- Generic Name
- permanent pacemaker Electrode
- Regulation Number
- 870.3680
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 25, 1986
- Date Received
- September 11, 1986
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Other
- Expedited Review
- N
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 |
|---|---|---|---|
| DTB | Permanent Pacemaker Electrode | FDA class 3 | Cardiovascular |