Atlas FDA

IMPELLA CONTROLLER WITH FLOW CONTROL

FDA 510(k) clearance K110845 · decided 2011-04-27

Clearance details

K-number
K110845
Device name
IMPELLA CONTROLLER WITH FLOW CONTROL
Applicant
Abiomed, Inc.
Decision
Substantially Equivalent
Date received
2011-03-28
Decision date
2011-04-27
Days to decision
30 days
Clearance type
Special
Product code
KFM
Device class
2
Regulation number
870.4360
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Danvers, MA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Impella CP with SmartAssist; Impella 5.5 with SmartAssist (P140003/S136)Abiomed, Inc.2025-12-19
Impella CP with SmartAssist; Impella 5.5 with SmartAssist (P170011/S062)Abiomed, Inc.2025-12-19
Impella 5.5 with SmartAssist (P140003/S131)Abiomed, Inc.2025-10-01
Impella CP with SmartAssist (P140003/S130)Abiomed, Inc.2025-09-24
Impella 2.5; Impella CP; Impella CP with SmartAssist; Impella 5.0; Impella 5.5 with SmartAssist; Impella LD (P140003/S129)Abiomed, Inc.2025-09-19
Impella RP, Impella RP with SmartAssist, Impella RP Flex with SmartAssist (P170011/S060)Abiomed, Inc.2025-09-19
Purge Cassette (P170011/S058)Abiomed, Inc.2025-09-15
Impella 5.5 with SmartAssist, Impella CP with SmartAssist, Purge Cassette (P140003/S126)Abiomed, Inc.2025-09-15