SYMBION CENTRIFUGAL BLOOD PUMP MODEL I— 510(k) K882129
Substantially EquivalentSymbion, Inc.
FDA 510(k) clearance K882129 for SYMBION CENTRIFUGAL BLOOD PUMP MODEL I, Substantially Equivalent on 1988-11-03. Applicant: Symbion, Inc.. Device class: 2.
Clearance details
- Applicant
- Symbion, Inc.
- Product code
- Code KFM
- Device class
- Class 2
- Regulation
- 21 CFR 870.4360
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code KFM
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More clearances from Symbion, Inc.
view allAdverse events under product code KFM
product code KFM- Death
- 109
- Injury
- 241
- Malfunction
- 1,779
- Total
- 2,129
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.