Medical Equipment Device Specialists is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Equipment Device Specialists - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medical Equipment Device Specialists has 6 FDA 510(k) cleared medical devices. Based in San Juan Capistrano, US.
Historical record: 6 cleared submissions from 2003 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medical Equipment Device Specialists Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Equipment Device Specialists
6 devices
Cleared
Apr 27, 2004
MODEL GST-1
Neurology
90d
Cleared
Oct 03, 2003
MEDS-4-INF+
Neurology
93d
Cleared
Jan 13, 2003
MEDS-4 NEUROMUSCULAR STIMULATOR
Neurology
90d
Cleared
Jan 13, 2003
MEDS-4 NEUROMUSCULAR STIMULATOR
Physical Medicine
90d
Cleared
Jan 13, 2003
MEDS-3 NEUROMUSCULAR STIMULATOR
Neurology
90d
Cleared
Jan 13, 2003
MEDS-3 NEUROMUSCULAR STIMULATOR
Physical Medicine
90d