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FDA 510(k) Applications Submitted by JG MEDICAL PRODUCTS LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070021
01/03/2007
ITALITE , MODEL 500-3.1, 550-3.1, 600-3.1, 650-3.1, 450-2.0,400-2.0
JG MEDICAL PRODUCTS LLC
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