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
Cleared
Aug 29, 1988
MEDIPAC II EC (TM), MODEL 7900
Neurology
52d
Cleared
Aug 04, 1987
ULTRAPAC II SX PLUS (TM)
Neurology
28d
Cleared
Mar 13, 1987
BACPAC (TM), MODEL 6500
Neurology
81d
Cleared
Aug 18, 1986
ULTRAPAC II SD (TM)
Neurology
59d
Cleared
Aug 01, 1986
ULTRAHESIVE II POSTOP ELECTRODE
Neurology
65d
Cleared
Feb 28, 1986
FASTENS(TM)
Neurology
123d
Cleared
Feb 14, 1986
MINIPAC PERSONAL TOUCH (TM)
Neurology
79d
Cleared
Jan 21, 1986
MINIPAC (TM)
Neurology
85d
Cleared
Jun 18, 1985
TRANSCUTANEOUS ELECTRICAL NERVE STIMULA-ELECTORDE
Neurology
85d
Cleared
Jun 08, 1983
SPEC IISX
Neurology
37d
Cleared
Mar 13, 1981
NEUROPAC ULTRA I
Neurology
8d
Cleared
Nov 22, 1978
NEUROPAC ULTRA II
Neurology
23d