FDA 510(k) Applications Submitted by RICHARD J CLARK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K961088 | 03/19/1996 | NON-CORING NEEDLE | ARROW INTL., INC. |
| K955819 | 12/26/1995 | A2 DETACHED DUAL PORT SYSTEM | ARROW INTL., INC. |
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