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Huntleigh Diagnostics , Ltd.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K020390 MODIFICATION TO FETAL ASSISTLQK2002-04-19 View
510(k) K002548 FETAL ASSISTHGM2001-03-06 View
510(k) K001677 BABY DOPPLEX 4000 (BD4000)HGM2000-08-14 View
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