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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