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FDA 510(k) Applications Submitted by INTERCURE LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020399
02/06/2002
RESPERATE; MODEL RR-150
INTERCURE LTD.
K000405
02/07/2000
INTERCURE LTD. RESPI-LOW
INTERCURE LTD.
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