
Medtronic Vascular
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ADD'L LABELING TO MINIX MODELS AND MINIX ST MODELS is an FDA 510(k)-cleared medical device (K895495) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 25, 1989. Regulation: 8.

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