La Jolla Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
La Jolla Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
La Jolla Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1987. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by La Jolla Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - La Jolla Technology, Inc.
5 devices
Cleared
Apr 01, 1987
DYNEX DISPOSABLE SELF-ADHERING ELECTRODE W/TENS
Neurology
78d
Cleared
Mar 09, 1987
DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.
Neurology
81d
Cleared
Jan 10, 1986
DYNEX REUSABLE, SELF-ADHERING ELECTRODE W/TENS
Neurology
86d
Cleared
Jan 18, 1984
ECG INTERFERENCE FILTER TF-03
Cardiovascular
145d
Cleared
Apr 18, 1983
NYNEX II
Neurology
26d