GEN 2 S-ICD & SQ-RX PULSE GENERATOR, SUBCUTANEOUS IMPLANTABLE CARDIOVERTER DEFRILLATOR
FDA premarket approval P110042/S052 · decided 2015-10-21
Approval details
- PMA number
- P110042
- Supplement
- S052
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- GEN 2 S-ICD & SQ-RX PULSE GENERATOR, SUBCUTANEOUS IMPLANTABLE CARDIOVERTER DEFRILLATOR
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific Corporation
- Date received
- 2015-09-30
- Decision date
- 2015-10-21
- Days to decision
- 21 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- ELIMINATE AN EQUIPMENT CHECK PERFORMED ON EQUIPMENT USED TO TEST PARYLENE COATING THICKNESS OF BATTERIES AND CAPACITORS USED IN THE DEVICE MODELS.
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