FDA 510(k) Applications Submitted by ARLENE DUTCHIK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970855 | 03/10/1997 | CLAVE CONNECTOR | ICU MEDICAL, INC. |
| K972712 | 07/21/1997 | CORE RESISTANT HUBER INFUSION SETS | ICU MEDICAL, INC. |
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