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Compass Intl., Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K964229 REGULUS NAVIGATORHAW1997-08-19 View
510(k) K935456 REGULUS MEASUREMENT UNITHAW1995-10-13 View
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