Medical Device Manufacturer · US , Deerpark , NY

Futuremed Div. of Future Impex Corp. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1985

Total

Cleared

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

1-12 of 17

Cleared Feb 10, 1994

UPGRADED SPIROMETER ST-90

K933511 · BTY

Anesthesiology · 210d

Cleared Nov 24, 1993

SELECTOR SL 01

K933220 · EWO

Ear, Nose, Throat · 146d

Cleared Nov 01, 1993

AUDIOMETER DA 323

K933222 · EWO

Ear, Nose, Throat · 123d

Cleared Oct 26, 1990

MEGA-TENS DUAL CHANNEL T.E.N.S.

K903017 · GZJ

Neurology · 108d

Cleared Jul 23, 1990

SPIRO ANALYZER MODEL ST 250

K901308 · BZG

Anesthesiology · 125d

Cleared Jul 27, 1989

TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR

K884972 · GZJ

Neurology · 239d

Cleared Jan 22, 1988

MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT

K871421 · IPF

Physical Medicine · 288d

Cleared Dec 02, 1987

SPIRO ANALYZER ST-300

TENS DEVICE FOR RELIEF OF CHRONIC PAIN

K864114 · GZJ

Neurology · 162d

Futuremed Div. of Future Impex Corp. - FDA 510(k) Cleared Devices

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