FDA 510(k) Applications Submitted by PRUCKA ENGINEERING, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960321 | 01/22/1996 | CARDIOCATH CATHETERIZATION LAB SYSTEM | PRUCKA ENGINEERING, INC. |
| K993414 | 10/12/1999 | PRUCKA ENGINEERING INC. CARDIOLAB EP SYSTEM,VERSION 4.2 | PRUCKA ENGINEERING, INC. |
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