FDA 510(k) Applications Submitted by PCK ELECTRONIC INDUSTRY AND TRADE CO, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011106 | 04/11/2001 | STONELITH, MODEL V5 | PCK ELECTRONIC INDUSTRY AND TRADE CO, LTD |
| K011311 | 04/30/2001 | UROLOGIC | PCK ELECTRONIC INDUSTRY AND TRADE CO, LTD |
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