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.

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

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