ClearanceBrief
Company ยท US

American Institute of Koryo Hand Therapy

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 1998. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MQXNeedle, Acupuncture, Single Use5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 9, 1998K980472KHT SOFT NEEDLE, ACUPUNCTURE NEEDLE
American Institute of Koryo Hand Therapy
MQX
Apr 9, 1998K980471KHT GUAM NEEDLE, ACUPUNCTURE NEEDLE
American Institute of Koryo Hand Therapy
MQX
Apr 6, 1998K980470KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
American Institute of Koryo Hand Therapy
MQX
Apr 3, 1998K980469KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
American Institute of Koryo Hand Therapy
MQX
Jan 13, 1998K974527KHT SEOAM NEEDLE, HAND ACUPUNCTURE NEEDLE
American Institute of Koryo Hand Therapy
MQX

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes