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Symbion, Inc.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
SYMBION CENTRIFUGAL BLOOD PUMP MODEL I (K882129)Symbion, Inc.1988-11-03
SUTURELESS TEMPORARY EPICARDIAL PACING LEAD (K873474)Symbion, Inc.1987-10-07

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Every clearance here is in the API, with alerts when new ones post.