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FDA 510(k) Applications Submitted by JAMES WHITE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K052647
09/26/2005
CLINI-LASE SYSTEM, MODELS CL-BASE, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-BASE, CLP-275, CLP-55.
AMERICAN SPINE CENTER, LTD.
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