American Institute of Koryo Hand Therapy is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Institute of Koryo Hand Therapy - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Institute of Koryo Hand Therapy has 5 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 5 cleared submissions from 1998 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by American Institute of Koryo Hand Therapy Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Institute of Koryo Hand Therapy
5 devices
Cleared
Apr 09, 1998
KHT GUAM NEEDLE, ACUPUNCTURE NEEDLE
General Hospital
62d
Cleared
Apr 09, 1998
KHT SOFT NEEDLE, ACUPUNCTURE NEEDLE
General Hospital
62d
Cleared
Apr 06, 1998
KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
General Hospital
59d
Cleared
Apr 03, 1998
KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
General Hospital
56d
Cleared
Jan 13, 1998
KHT SEOAM NEEDLE, HAND ACUPUNCTURE NEEDLE
General Hospital
42d