Rln Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rln Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rln Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in Jefferson City, US.
Historical record: 5 cleared submissions from 1989 to 2001. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Rln Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rln Systems, Inc.
5 devices
Cleared
Jan 16, 2001
LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET
Ear, Nose, Throat
43d
Cleared
Dec 22, 1995
NERVE LOCATOR/MONITOR SYSTEM MODIFICATION
Ear, Nose, Throat
101d
Cleared
Nov 24, 1992
RLN NERVE LOCATOR/MONITOR
Ear, Nose, Throat
53d
Cleared
Sep 30, 1992
NERVE LOCATOR/MONITOR SYSTEM, MODIFICATION
Ear, Nose, Throat
482d
Cleared
Dec 08, 1989
HEMOSTAT/STIMULATOR PROBE
Ear, Nose, Throat
79d