Haag-Streit AG is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Haag-Streit AG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Haag-Streit AG has 4 FDA 510(k) cleared medical devices. Based in Wadsworth, US.
Historical record: 4 cleared submissions from 1998 to 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Haag-Streit AG Filter by specialty or product code using the sidebar.
Haag-Streit AG — FDA 510(k) Products and Clearance History
4 devices
Cleared
Sep 10, 2014
EyeSuite Imaging
Ophthalmic
13d
Cleared
Mar 19, 2010
SLIT LAMP BO 900, BQ 900, BP900
Ophthalmic
53d
Cleared
Oct 20, 2009
LENSTAR, MODEL LS900
Ophthalmic
385d
Cleared
Aug 14, 1998
BC 900 SLIT LAMP
Ophthalmic
64d