Solcoor, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Solcoor, Inc. has 7 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 7 cleared submissions from 1985 to 1989. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Solcoor, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solcoor, Inc.
7 devices
Cleared
Oct 18, 1989
AGAR 3K NEUROMUSCULAR STIMULATOR
Physical Medicine
495d
Cleared
Oct 16, 1989
AGAR 4000 NEUROMUSCULAR STIMULATOR
Physical Medicine
493d
Cleared
Mar 25, 1987
AGAR 7K TENS INSTRUMENT
Neurology
271d
Cleared
Sep 09, 1986
AGAR 9K TENS
Neurology
116d
Cleared
Sep 09, 1986
UNI-TENS
Neurology
116d
Cleared
Sep 09, 1986
UNI-TENS XL TENS
Neurology
116d
Cleared
Oct 29, 1985
PEAK FLOWMETERS FOR SPIROMETRY
Anesthesiology
214d