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FDA 510(k) Applications Submitted by JOYCE HEINRICH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091726
06/11/2009
NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980
USA LASER BIOTECH INC.
K014208
12/21/2001
SSIR SYSTEM
RUSSIAN-AMERICAN TECHNOLOGY ASSOCIATES, INC.
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