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FDA 510(k) Applications Submitted by DEEP BREEZE LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091732
06/11/2009
VRLXP, MODEL XP
DEEP BREEZE LTD.
K073582
12/20/2007
VRIICU SYSTEM
DEEP BREEZE LTD.
K061495
05/31/2006
VR LUNG ELECTROSONOGRAPH
DEEP BREEZE LTD.
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