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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