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FDA 510(k) Applications Submitted by DIDECO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K004001
12/26/2000
MONOLYTH MIMESYS HOLLOW FIBER OXYGENATOR
DIDECO
K010478
02/20/2001
DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR
DIDECO
K001388
05/02/2000
DATA MASTER PERFUSION MONITORING SYSTEM
DIDECO
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