Aerotel, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Aerotel, Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Aerotel, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Israel, IL.
Historical record: 6 cleared submissions from 1994 to 1998. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Aerotel, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aerotel, Ltd.
6 devices
Cleared
Jun 16, 1998
HEARTVIEW P12/8 ELECTROCARDIOGRAPH RECORDER AND TRANSMITTER
Cardiovascular
152d
Cleared
Jul 18, 1996
HEART 400 ECG TRANSMITTER
Cardiovascular
342d
Cleared
Jul 10, 1996
AEROTEL TELELINK ECG TELEPHONIC RECEIVING INTERFACE
Cardiovascular
92d
Cleared
Oct 24, 1995
HEARTVIEW(TM) 12-LEAD ELECTROCARDIOGRAPH RECORDER/TRANSMITTER
Cardiovascular
294d
Cleared
Jan 11, 1995
HEART 1001
Cardiovascular
684d
Cleared
Mar 18, 1994
HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE
Cardiovascular
420d