FDA 510(k) Applications Submitted by ATLANTIS DIAGNOSTICS INTL., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K980860 03/05/1998 HDI 1000 DIAGNOSTIC ULTRASOUND SYSTEM ATLANTIS DIAGNOSTICS INTL., INC.
K961073 03/18/1996 ATLAS 2.0 & HITACHI 2.0 (A TRADE NAME SUBJECT TO CHANGE) ATLANTIS DIAGNOSTICS INTL., INC.


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