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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