FDA 510(k) Applications Submitted by DANIEL YE HUA

FDA 510(k) Number Submission Date Device Name Applicant
K990406 02/09/1999 KINGLI ACUPUNCTURE NEEDLE UNITED PACIFIC CO., LTD.
K001718 06/05/2000 MILLENNIA ACUPUNCTURE NEEDLE UNITED PACIFIC CO., LTD.
K003010 09/26/2000 SPIRIT ACUPUNCTURE NEEDLE UNITED PACIFIC CO., LTD.
K991503 04/29/1999 SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 UNITED PACIFIC CO., LTD.
K993123 09/20/1999 QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B UNITED PACIFIC CO., LTD.


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