Medical Consultants Intl. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Consultants Intl. , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medical Consultants Intl. , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Glen Rock, US.
Historical record: 6 cleared submissions from 1990 to 1991. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medical Consultants Intl. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Consultants Intl. , Ltd.
6 devices
Cleared
May 09, 1991
MODEL SW-103 SOLITANS STIMULATOR
Neurology
233d
Cleared
Dec 17, 1990
MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)
Dental
305d
Cleared
Oct 04, 1990
LISS CRANIAL STIMULATOR MODEL SBL202-B
Neurology
90d
Cleared
Sep 07, 1990
MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC
Neurology
63d
Cleared
May 03, 1990
LISS CRANIAL STIMULATOR MODEL SBL201-M
Neurology
288d
Cleared
Apr 10, 1990
LISS BODY STIMULATOR MODEL SBL501-M
Neurology
161d