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Impella RP System; Impella RP with SmartAssist System; Impella RP Flex with SmartAssist System;

FDA premarket approval P170011/S056 · decided 2025-08-01

Approval details

PMA number
P170011
Supplement
S056
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
Impella RP System; Impella RP with SmartAssist System; Impella RP Flex with SmartAssist System;
Generic name
Temporary non-roller type right heart support blood pump
Applicant
Abiomed, Inc.
Date received
2025-02-07
Decision date
2025-08-01
Days to decision
175 days
Decision code
APPR
Product code
PYX
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
approval for modifying the Impella labeling to reflect the findings of the Impella Sodium Bicarbonate Post-Approval Study

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510(k) clearances by this applicant

RecordFirmDate
14Fr Low Profile Introducer Kit (K252766)Abiomed, Inc.2025-10-08
Abiomed 14Fr Low Profile Introducer Kit (K241708)Abiomed, Inc.2024-08-06
preCARDIA Occlusion System (K221294)Abiomed, Inc.2023-06-30
OXY-1 System (K223161)Abiomed, Inc.2023-02-23
Abiomed 14Fr Low Profile Introducer Set (K222113)Abiomed, Inc.2022-10-13
Impella XR Sheath Set (K202330)Abiomed, Inc.2020-12-07
OXY-1 System (K200109)Abiomed, Inc.2020-10-23
Abiomed 23 Fr Sheath (K201116)Abiomed, Inc.2020-06-15