Sendx Medical, Inc. is one of 13027 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sendx Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ABL80 FLEX and ABL80 FLEX CO-OX, ABL80 FLEX CO-OX with AQURE connectivity, ABL80 FLEX ANALYZER
6
Total
6
Cleared
0
Denied
Sendx Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 6 cleared submissions from 1997 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Sendx Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Radiometer Medical Aps as regulatory consultant.
FDA 510(k) Regulatory Record - Sendx Medical, Inc.
6 devices
Cleared
Dec 07, 2015
ABL80 FLEX and ABL80 FLEX CO-OX
Chemistry
172d
Cleared
Aug 06, 2015
ABL80 FLEX CO-OX with AQURE connectivity
Chemistry
29d
Cleared
Jul 31, 2008
ABL 80 CO-OX SYSTEM
Chemistry
170d
Cleared
Nov 01, 2005
ABL80 FLEX ANALYZER
Chemistry
119d
Cleared
Feb 01, 2000
ABL 77 PH, BLOOD GAS AND ELECTROLYTE ANALYSIS SYSTEM
Chemistry
40d
Cleared
Dec 03, 1997
SENDX 100 PH, BLOOD GAS AND ELECTROLYTE ANALYSIS SYSTEM
Chemistry
63d