Medical Device Manufacturer · US , Mahwah , NJ

Dantec Medical, Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1990

Total

Cleared

Denied

Dantec Medical, Inc. has 25 FDA 510(k) cleared medical devices. Based in Mahwah, US.

Historical record: 25 cleared submissions from 1990 to 1996. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Dantec Medical, Inc. Filter by specialty or product code using the sidebar.

Dantec Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dantec Medical, Inc.

25 devices

1-12 of 25

Cleared Sep 16, 1996

DANTEC DUET

K960503 · FEN

Gastroenterology & Urology · 227d

Cleared Mar 25, 1996

DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)

Gastroenterology & Urology · 89d

NEEDLE ELECTRODES AND DISPOSABLE SCALP ELECTRODE

K932059 · IKT

Neurology · 523d

Cleared Sep 26, 1994

DANTEC 13R45 BAR ELECTRODE

K934580 · GXY

Neurology · 368d

Cleared Mar 30, 1994

DANTEC DISPOSABLE CONCENTRIC NEEDLE

K931966 · IKT

Neurology · 343d

Cleared Nov 09, 1993

DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE)

K931923 · GWF

Neurology · 207d

Cleared Aug 31, 1993

DANTEC MAGNETIC STIMULATOR MAGPRO

Dantec Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Dantec Medical, Inc.

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