Reynolds Medical , Ltd. is one of 14651 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reynolds Medical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EVENTSTATION ECG TRANS-TELEPHONIC RECEIVING SYSTEM, CARDIOCALL CARDIAC EVENT RECORDER, PATHFINDER 700 HOLTER ANALYZER
12
Total
12
Cleared
0
Denied
Reynolds Medical , Ltd. has 12 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1982 to 2003.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reynolds Medical , Ltd.
12 devices
Cleared
Aug 01, 2003
CARDIODIRECT, MODELS 12M, 12I, 12S
Cardiovascular
221d
Cleared
Dec 13, 2001
CARDIOCOLLECT PORTABLE ELECTROCARDIOGRAPH
Cardiovascular
64d
Cleared
Jul 20, 2001
CARDIONAVIGATOR INFORMATION MANAGEMENT SYSTEM
Cardiovascular
79d
Cleared
Jul 13, 2001
LIFECARD CF 7 DAY
Cardiovascular
31d
Cleared
Apr 19, 2000
LIFECARD CF COMPACT RECORDER
Cardiovascular
20d
Cleared
Jul 08, 1999
EVENTSTATION ECG TRANS-TELEPHONIC RECEIVING SYSTEM
Cardiovascular
90d
Cleared
Dec 04, 1997
CARDIOCALL CARDIAC EVENT RECORDER
Cardiovascular
142d
Cleared
Jul 15, 1996
PATHFINDER 700 HOLTER ANALYZER
Cardiovascular
448d
Cleared
Oct 20, 1994
TRACKER 2/TRACKER 3 HOLTER RECORDER
Cardiovascular
105d
Cleared
Oct 30, 1989
E-RAM
Cardiovascular
395d
Cleared
Oct 20, 1987
PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR
Cardiovascular
197d
Cleared
May 28, 1982
TRACKER-2 CHANNEL ECG TAPE RECORDER
Cardiovascular
7d