FDA 510(k) Applications Submitted by LINDA SLUTZKY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133074 | 09/30/2013 | MEGA 8FR. 50CC AND SENSATION PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETERS AND ACCESSORIES | DATASCOPE CORP. |
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