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Dickstein, Shapiro & Morin

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K863538 RESPICENTRAL(TM)BZK1986-09-24 View
510(k) K861326 RESPISOMNOGRAPHBZQ1986-06-13 View
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