FDA 510(k) Applications Submitted by CARDIO DESIGN PTY. LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K983052 | 09/01/1998 | PERITRON PERINEOMETER MODEL 9300V OR 9300A | CARDIO DESIGN PTY. LTD. |
| K945611 | 11/15/1994 | PERITRON | CARDIO DESIGN PTY. LTD. |
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