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Atlantis Diagnostics Intl., Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980860 HDI 1000 DIAGNOSTIC ULTRASOUND SYSTEMIYO1998-04-02 View
510(k) K961073 ATLAS 2.0 & HITACHI 2.0 (A TRADE NAME SUBJECT TO CHANGE)IYO1997-02-19 View
510(k) K936067 ATLAS 1.0 DIAGNOSTIC ULTRASOUND SYSTEMIYN1995-10-27 View
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