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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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