FDA 510(k) Applications Submitted by JAMES W HELLER

FDA 510(k) Number Submission Date Device Name Applicant
K022821 08/26/2002 ARAGON WIRING SYSTEM WIRE CARTRIDGE, MODELS I0007 WIRE CARTRIDGE, 22 GAUGE, I0008 WIRE CARTRIDGE, 24 GAUGE, I0009 WIRE E IDEATRICS, INC.


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