Amuchina Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amuchina Intl., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Amuchina Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 5 cleared submissions from 1986 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Amuchina Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amuchina Intl., Inc.
5 devices
Cleared
Jan 10, 2000
AMUKIN D
Gastroenterology & Urology
209d
Cleared
Jul 26, 1995
AMUCHINA
General Hospital
71d
Cleared
Jul 09, 1987
MODIFIED LABELING FOR AMUKIN-50%
Gastroenterology & Urology
77d
Cleared
Mar 09, 1987
AMUKIN-50% FOR CAPD Y-SET
Gastroenterology & Urology
220d
Cleared
May 13, 1986
AMUCHINA/DIALYZER DISINFECTANT
Gastroenterology & Urology
343d