Rigel Medical Electronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rigel Medical Electronics, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Rigel Medical Electronics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mill Valley, US.
Historical record: 6 cleared submissions from 1984 to 1989. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rigel Medical Electronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rigel Medical Electronics, Inc.
6 devices
Cleared
Feb 02, 1989
PATIENT MONITOR RIGEL MODEL MULTICARE 429
Cardiovascular
87d
Cleared
Jun 28, 1988
RIGEL MODEL MULTICARE 409
Cardiovascular
196d
Cleared
Apr 18, 1985
NEONATAL MONITOR 309
Cardiovascular
73d
Cleared
Mar 01, 1985
ECG PATIENT MONITOR 302
Cardiovascular
45d
Cleared
Mar 01, 1985
ECG PATIENT MONITOR 301
Cardiovascular
45d
Cleared
Dec 27, 1984
ECG PATIENT MONITOR
Cardiovascular
121d