Company · US

Dr. Franz Kohler Chemie GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2020. 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

Code	Device	Records
KDL	Set, Perfusion, Kidney, Disposable	3
KDN	System, Perfusion, Kidney	1
MSB	System And Accessories, Isolated Heart, Transport And Preservation	1

Decided	510(k)	Device and applicant	Code
Apr 24, 2020	K192408	Custodiol HTK Solution Dr. Franz Kohler Chemie GmbH, DE	KDL
Feb 28, 2005	K043461	CUSTODIOL Dr. Franz Kohler Chemie GmbH	KDL
Apr 5, 2004	K032794	CUSTODIOL Dr. Franz Kohler Chemie GmbH	MSB
Jan 6, 2003	K020924	CUSTODIOL HTK SOLUTION Dr. Franz Kohler Chemie GmbH	KDL
Dec 10, 1999	K992209	CUSTODIOL Dr. Franz Kohler Chemie GmbH	KDN

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.