Atlas FDA

RELAY/DASH/STRIDE/DART PACING SYSTEMS

FDA premarket approval P910020/S010 · decided 1996-03-15

Approval details

PMA number
P910020
Supplement
S010
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
RELAY/DASH/STRIDE/DART PACING SYSTEMS
Generic name
implantable pacemaker Pulse-generator
Applicant
Boston Scientific
Date received
1995-08-29
Decision date
1996-03-15
Days to decision
199 days
Decision code
APPR
Product code
DXY
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
ALTERNATE ACCELEROMETER

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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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WallFlex Biliary PLUS RX Stent System (K242950)Boston Scientific2024-12-06
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Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System (K233939)Boston Scientific2024-04-29