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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