Dr. Franz Kohler Chemie GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dr. Franz Kohler Chemie GmbH - FDA 510(k) Cleared Devices
Recent clearances: Custodiol HTK Solution
5
Total
5
Cleared
0
Denied
Dr. Franz Kohler Chemie GmbH has 5 FDA 510(k) cleared medical devices. Based in Brookeville, US.
Historical record: 5 cleared submissions from 1999 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dr. Franz Kohler Chemie GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dr. Franz Kohler Chemie GmbH
5 devices
Cleared
Apr 24, 2020
Custodiol HTK Solution
Gastroenterology & Urology
233d
Cleared
Feb 28, 2005
CUSTODIOL
Gastroenterology & Urology
75d
Cleared
Apr 05, 2004
CUSTODIOL
Gastroenterology & Urology
210d
Cleared
Jan 06, 2003
CUSTODIOL HTK SOLUTION
Gastroenterology & Urology
291d
Cleared
Dec 10, 1999
CUSTODIOL
Gastroenterology & Urology
163d