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Medi-Dyne, Inc.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER (K000825)Medi-Dyne, Inc.2000-09-21
MEDI-DYNE GUIDING CATHETER (K970401)Medi-Dyne, Inc.1997-08-01
MODIFIED LUER (K931833)Medi-Dyne, Inc.1993-09-28
MEDI-DYNE ANGIOGRAPHIC CATHETER (K930694)Medi-Dyne, Inc.1993-08-02

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Every clearance here is in the API, with alerts when new ones post.