Haag-Streit AG is one of 18904 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
Recent clearances: EyeSuite Imaging, SLIT LAMP BO 900, BQ 900, BP900, LENSTAR, MODEL LS900
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.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Haag-Streit AG
4 devices