L.O.N. Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
L.O.N. Research, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
L.O.N. Research, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 1989. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by L.O.N. Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - L.O.N. Research, Inc.
5 devices
Cleared
Jul 14, 1989
DISPOSABLE TRANSDUCER MANIFOLD
Cardiovascular
155d
Cleared
Mar 22, 1988
ANGIOPLASTY BALLOON INFLATION DEVICE
Cardiovascular
69d
Cleared
Dec 03, 1985
L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION
Cardiovascular
133d
Cleared
Dec 02, 1981
L.O.N. REUSABLE MANIFOLDS & STOPCOCKS
Cardiovascular
103d
Cleared
Dec 02, 1981
L.O.N. DISPOSABLE CORONARY MANIFOLD
Cardiovascular
103d