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FDA 510(k) Applications Submitted by PCK ELECTRONIC INDUSTRY & TRADE CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K061350
05/15/2006
LITHODIAMOND ULTRA
PCK ELECTRONIC INDUSTRY & TRADE CO., LTD.
K053279
11/23/2005
UROVANTAGE
PCK ELECTRONIC INDUSTRY & TRADE CO., LTD.
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