LIVEWIRE TC ABLATION CATHETER
FDA premarket approval P960016/S046 · decided 2015-04-09
Approval details
- PMA number
- P960016
- Supplement
- S046
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- LIVEWIRE TC ABLATION CATHETER
- Generic name
- Cardiac ablation percutaneous catheter
- Applicant
- St Jude Medical
- Date received
- 2014-04-30
- Decision date
- 2015-04-09
- Days to decision
- 344 days
- Decision code
- APPR
- Product code
- LPB
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minnetonka, MN
- Statement
- APPROVAL FOR A ST. JUDE MEDICAL MANUFACTURING SITE LOCATED AT ST. PAUL, MN TO SERVICE AND REPAIR THE 1500T SERIES RF GENERATORS.
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