Medical Devices, Inc. - FDA 510(k) Cleared Devices
49
Total
47
Cleared
0
Denied
24 devices
Cleared
Dec 05, 1994
SMARTBRACE ELECTRODE
Neurology
335d
Cleared
Dec 05, 1994
ELECTROFLEX
Neurology
159d
Cleared
Mar 14, 1994
HOME MICROCURRENT HMC
Neurology
137d
Cleared
Feb 23, 1994
FLEXMATE
Neurology
149d
Cleared
Jun 24, 1991
SX90 (TM),MODEL 4800S
Neurology
27d
Cleared
Mar 27, 1991
MC II (TM), MODEL 7200S
Neurology
252d
Cleared
Dec 08, 1989
DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S
Neurology
88d
Cleared
May 24, 1989
IF-II (TM), MODEL 9800
Neurology
282d
Cleared
Mar 09, 1989
MEDIMOD(TM), MODEL 8900
Neurology
27d
Cleared
Sep 30, 1988
MULTIDAY, MODELS 8300 AND 8310
Neurology
81d
Cleared
Sep 29, 1988
PROGEL (TM) DUAL ELECTRODE PAD, MODEL 8535
Neurology
80d
Cleared
Sep 29, 1988
PROGEL(TM), MODELS 8630 AND 8635
Neurology
80d