Cardiovascular Diagnostic Services is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiovascular Diagnostic Services - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cardiovascular Diagnostic Services has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1981 to 1996. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Cardiovascular Diagnostic Services Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiovascular Diagnostic Services
8 devices
Cleared
Mar 18, 1996
TAS PTONE
Hematology
83d
Cleared
Nov 15, 1993
TAS ANALYZER
Hematology
144d
Cleared
Jan 25, 1991
COAG-1 PT-NC TEST CARD
Hematology
127d
Cleared
Aug 01, 1990
MODIFIED COAG-1 PT TEST CARD
Hematology
21d
Cleared
May 22, 1989
COAG-1 APTT TEST CARD
Hematology
83d
Cleared
Aug 25, 1988
COAG-I ANALYZER, ALPHA MODEL
Hematology
72d
Cleared
Aug 25, 1988
COAG-I PT TEST CARD
Hematology
72d
Cleared
Oct 13, 1981
DORROS-SPRING PRESSURIZER
Cardiovascular
56d