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Anatros Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K833520 RATEMINDER II SPECIALTY CARELDR1983-12-22 View
510(k) K812233 RATEMINDERLDR1981-08-25 View
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