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Cardiac Assist, Maquet Cardiovascular, LLC

FDA Regulatory Profile

Cardiac Assist, Maquet Cardiovascular, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 15, 2011.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K112372CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMPSeptember 15, 2011
K112327SENSATION(TM) PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIESSeptember 9, 2011

FDA data resources