Data Critical Corp. is one of 7279 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Data Critical Corp. - FDA 510(k) Cleared Devices
Recent clearances: CARDIO-PAGER SYSTEM, RHYTHMSTAT XL
9
Total
9
Cleared
0
Denied
Data Critical Corp. has 9 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 9 cleared submissions from 1997 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Data Critical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Data Critical Corp.
9 devices
Cleared
Oct 19, 2001
MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM
Cardiovascular
28d
Cleared
Jul 24, 2001
MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM
Cardiovascular
27d
Cleared
Jul 24, 2001
MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM
Cardiovascular
27d
Cleared
Apr 05, 2001
ALARMVIEW WIRELESS DATA NETWORK SYSTEM
Cardiovascular
9d
Cleared
Mar 07, 2001
FLEXVIEW CLINICAL MONITORING SYSTEM
Cardiovascular
71d
Cleared
Nov 19, 1999
ALARMVIEW SYSTEM
Cardiovascular
87d
Cleared
Sep 20, 1999
STATVIEW SYSTEM
Cardiovascular
224d
Cleared
Mar 31, 1998
CARDIO-PAGER SYSTEM
Cardiovascular
194d
Cleared
Dec 04, 1997
RHYTHMSTAT XL
Cardiovascular
212d