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Impella RP, Impella RP with Smart Assist, Impella $.0/LD

FDA premarket approval P170011/S049 · decided 2023-04-27

Approval details

PMA number
P170011
Supplement
S049
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Impella RP, Impella RP with Smart Assist, Impella $.0/LD
Generic name
Temporary non-roller type right heart support blood pump
Applicant
Abiomed, Inc.
Date received
2023-03-28
Decision date
2023-04-27
Days to decision
30 days
Decision code
APPR
Product code
PYX
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
Approval of the revised protocol for the Impella Real-World Surveillance of patients using Sodium Bicarbonate.

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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