EMBLEM S-ICD PULSE GENERATOR
FDA premarket approval P110042/S051 · decided 2015-10-19
Approval details
- PMA number
- P110042
- Supplement
- S051
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- EMBLEM S-ICD PULSE GENERATOR
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific Corporation
- Date received
- 2015-09-23
- Decision date
- 2015-10-19
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- CHANGE TO THE RADII PROFILE MEASUREMENT METHOD FOR THE FRONT AND BACK CASES OF THE ABOVE REFERENCED DEVICE.
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