COGNIS CARDIAC RESYNCHRONIZATION HE DEFIBRILLATOR
FDA premarket approval P010012/S194 · decided 2008-12-11
Approval details
- PMA number
- P010012
- Supplement
- S194
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- COGNIS CARDIAC RESYNCHRONIZATION HE DEFIBRILLATOR
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific Corp
- Date received
- 2008-11-06
- Decision date
- 2008-12-11
- Days to decision
- 35 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL FOR THE PROGRAMMER SW MODEL 2868 V1.04 AND NOMINAL PARAMETERS LOADED DURING MANUFACTURING.
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