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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