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FDA 510(k) Applications Submitted by CARE ELECTRONICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K043575
12/27/2004
DERMILLUME, MODEL PRO1000
CARE ELECTRONICS, INC.
K051681
06/23/2005
DERMILLUME RED, MODEL HR1000
CARE ELECTRONICS, INC.
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