Delbio Incorporation is one of 512 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Delbio Incorporation - FDA 510(k) Cleared Devices
Recent clearances: OXICARE FINGERTIP PULSE OXIMETER, DA01 BLOOD GLUCOSE MONITORING SYSTEM, DIATRUE PLUS BLOOD GLUCOSE MONITORING SYSTEM
7
Total
7
Cleared
0
Denied
Delbio Incorporation has 7 FDA 510(k) cleared medical devices. Based in Taoyuan, TW.
Historical record: 7 cleared submissions from 2011 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Delbio Incorporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Delbio Incorporation
7 devices
Cleared
Feb 28, 2014
OXICARE FINGERTIP PULSE OXIMETER
Anesthesiology
151d
Cleared
Oct 24, 2013
DA01 BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
90d
Cleared
Aug 23, 2013
DIATRUE PLUS BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
204d
Cleared
Dec 11, 2012
DA01 BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
264d
Cleared
Mar 13, 2012
DIATRUE PLUS BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
487d
Cleared
Feb 08, 2012
DIACHECK SMART/SUPERIOR BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
86d
Cleared
Sep 16, 2011
DIACHECK BLOOD GLUCOSE MONITORING SYSTEM MODEL: PREMIUM
Chemistry
543d