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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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