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Chest M.I., Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K090646 CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105BZG2009-07-23 View
510(k) K080921 SPIRO-MASTER PC-10 SPIROMETRY SYSTEMBZG2009-01-21 View
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