FDA 510(k) Applications Submitted by NORSELD PTY., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K032397 08/04/2003 DUAL YELLOW LASER, MODEL DUAL YELLOW D10B NORSELD PTY., LTD.
K023899 11/22/2002 DUAL YELLOW LASER, MODEL D10B NORSELD PTY., LTD.


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