Tuttnauer Co. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tuttnauer Co. , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Tuttnauer Co. , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1984 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tuttnauer Co. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tuttnauer Co. , Ltd.
6 devices
Cleared
Dec 08, 2011
TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES
General Hospital
171d
Cleared
Feb 02, 2007
TUTTNAUER PREVACUUM STEAM HEATED AUTOCLAVE, MODELS 6990 SP-1A, 66120 SP-1A,...
General Hospital
50d
Cleared
Feb 20, 2001
EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870
General Hospital
104d
Cleared
Jul 08, 1993
TUTTNAUER LSI (AUTOMATIC)
General Hospital
526d
Cleared
Jun 04, 1985
TUTTNAUER PRE-VACUUM AUTOCLAVE
General Hospital
132d
Cleared
Jan 11, 1984
AMERICAN GOLD SERIES AUTOCLAVE
General Hospital
69d