Kitazato Biopharma Co;Ltd is one of 4753 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kitazato Biopharma Co;Ltd - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Kitazato Biopharma Co;Ltd has 6 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 6 cleared submissions from 2012 to 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Kitazato Biopharma Co;Ltd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kitazato Biopharma Co;Ltd
6 devices
Cleared
Oct 07, 2016
Cryotop Vitrification Kit and Cryotop Thawing Kit
Obstetrics & Gynecology
192d
Cleared
Jul 28, 2016
PBS(-), Phosphate Buffered Saline
Obstetrics & Gynecology
121d
Cleared
Apr 21, 2016
MINERAL OIL
Obstetrics & Gynecology
91d
Cleared
Mar 14, 2016
Cryotop US
Obstetrics & Gynecology
150d
Cleared
Apr 03, 2014
CRYOTOP(R) SC
Obstetrics & Gynecology
80d
Cleared
Dec 12, 2012
CRYOTOP
Obstetrics & Gynecology
454d