FDA 510(k) Applications Submitted by VALLEY WEST, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990447 | 02/12/1999 | 1000 PRESSURE INFUSION SIGMACON 1000 | VALLEY WEST, INC. |
| K980089 | 01/09/1998 | 3600 PRESURE INFUSOR, SIGMACON 3600, LAPRO FLOW 3000 | VALLEY WEST, INC. |
| K973814 | 10/07/1997 | TRUMP-IT II AND MAGNUM 250 | VALLEY WEST, INC. |
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