Takagi Seiko Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Takagi Seiko Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Adelaide, South Australia, AU.
Historical record: 5 cleared submissions from 2007 to 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Takagi Seiko Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Takagi Seiko Co., Ltd.
5 devices
Cleared
Dec 10, 2018
Applanation tonometer AT-2
Ophthalmic
90d
Cleared
Oct 17, 2017
Applanation tonometer AT-1
Ophthalmic
36d
Cleared
Apr 14, 2017
Marco Ultra M3, Marco Ultra M4
Ophthalmic
205d
Cleared
May 26, 2016
Z5 Slit lamp microscope, Z2 Slit lamp microscope
Ophthalmic
265d
Cleared
Mar 13, 2007
ELLEX SLIT LAMP, MODEL 30XL
Ophthalmic
127d