Hmt, Inc. is one of 438 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Hmt, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HMT 21, HMT 2000 URINARY INCONTINENCE SYSTEM
1
Total
1
Cleared
0
Denied
Hmt, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hmt, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hmt, Inc.
1 devices