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INGEVITY™ MRI, INGEVITY™ +

FDA premarket approval P150012/S153 · decided 2025-08-22

Approval details

PMA number
P150012
Supplement
S153
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INGEVITY™ MRI, INGEVITY™ +
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Boston Scientific
Date received
2023-11-01
Decision date
2025-08-22
Days to decision
660 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
approval for changes to the cleaning equipment and solvent used to clean helices used in Boston Scientific Corporation cardiac leads

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510(k) clearances by this applicant

RecordFirmDate
OptiCross Coronary Imaging Catheter (H749518110); OptiCross 6 Coronary Imaging Catheter (H7495181160); OptiCross HD Coronary Imaging Catheter (H74939352040); OptiCross 6 HD Coronary Imaging Catheter (H74939354080); OptiCross Coronary Imaging Catheter (Bagless) (H749518130); OptiCross 6 Coronary Imaging Catheter (Bagless) (H7495181360); OptiCross HD Coronary Imaging Catheter (Bagless) (H74939352050); OptiCross 6 HD Coronary Imaging Catheter (Bagless) (H74939354090) (K260816)Boston Scientific2026-04-08
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