Futuremed Div. of Future Impex Corp. is one of 5796 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Futuremed Div. of Future Impex Corp. - FDA 510(k) Cleared Devices
Recent clearances: UPGRADED SPIROMETER ST-90, SELECTOR SL 01, AUDIOMETER DA 323
17
Total
17
Cleared
0
Denied
Futuremed Div. of Future Impex Corp. has 17 FDA 510(k) cleared medical devices. Based in Deerpark, US.
Historical record: 17 cleared submissions from 1985 to 1994.
Browse the FDA 510(k) cleared devices submitted by Futuremed Div. of Future Impex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Futuremed Div. of Future Impex Corp.
17 devices
Cleared
Feb 10, 1994
UPGRADED SPIROMETER ST-90
Anesthesiology
210d
Cleared
Nov 24, 1993
SELECTOR SL 01
Ear, Nose, Throat
146d
Cleared
Nov 01, 1993
AUDIOMETER DA 323
Ear, Nose, Throat
123d
Cleared
Oct 26, 1990
MEGA-TENS DUAL CHANNEL T.E.N.S.
Neurology
108d
Cleared
Jul 23, 1990
SPIRO ANALYZER MODEL ST 250
Anesthesiology
125d
Cleared
Jul 27, 1989
TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR
Neurology
239d
Cleared
Jan 22, 1988
MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT
Physical Medicine
288d
Cleared
Dec 02, 1987
SPIRO ANALYZER ST-300
Anesthesiology
72d
Cleared
Jul 16, 1987
CARBON ELECTRODE
Neurology
50d
Cleared
Jul 15, 1987
CONDUCTIVITY GEL
Neurology
58d
Cleared
Jul 15, 1987
CONDUCTIVITY GEL
Neurology
49d
Cleared
Apr 01, 1987
TENS DEVICE FOR RELIEF OF CHRONIC PAIN
Neurology
162d