DeviceClearance

CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP— 510(k) K112372

Substantially Equivalent

Cardiac Assist, Maquet Cardiovascular, LLC

FDA 510(k) clearance K112372 for CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP, Substantially Equivalent on 2011-09-15. Applicant: Cardiac Assist, Maquet Cardiovascular, LLC. Device class: 2.

Clearance details

Applicant
Cardiac Assist, Maquet Cardiovascular, LLC
Product code
Code DSP
Device class
Class 2
Regulation
21 CFR 870.3535
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Manwah, NJ, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DSP

product code DSP
Death
317
Injury
566
Malfunction
36,831
Other
4
Total
37,718

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K112372

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K112372.

Data sourced from openFDA. This site is unofficial and independent of the FDA.