United Pacific Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
United Pacific Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
United Pacific Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Alhambra, US.
Historical record: 5 cleared submissions from 1999 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by United Pacific Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - United Pacific Co., Ltd.
5 devices
Cleared
Oct 19, 2000
SPIRIT ACUPUNCTURE NEEDLE
General Hospital
23d
Cleared
Jun 21, 2000
MILLENNIA ACUPUNCTURE NEEDLE
General Hospital
16d
Cleared
Dec 17, 1999
QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D,...
Physical Medicine
88d
Cleared
Jul 28, 1999
SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36
Physical Medicine
90d
Cleared
Apr 16, 1999
KINGLI ACUPUNCTURE NEEDLE
General Hospital
66d