Medical Device Manufacturer · US , Walker , MI

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

12 submissions · 12 cleared · Since 1985

Total

Cleared

Denied

Dantec Electronics, Inc. has 12 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 12 cleared submissions from 1985 to 1990. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Dantec Electronics, Inc.

12 devices

1-12 of 12

Cleared Jun 18, 1990

CONCENTRIC ELECTRODE TYPE #13R01, 13R02

K895460 · IKT

Neurology · 285d

Cleared May 14, 1990

SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118

K894911 · GXZ

Neurology · 286d

Cleared Oct 04, 1989

DANTEC 22K60/61/62 CATHETER TIP TRANSDUCER

K884915 · FAP

Gastroenterology & Urology · 310d

Cleared Oct 17, 1988

DANTEC MAGNETIC STIMULATOR

K881915 · GWF

Neurology · 161d

Cleared Apr 14, 1988

DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE

K874758 · FAP

Gastroenterology & Urology · 148d

Cleared Apr 14, 1988

13L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLE

K874759 · FAP

Gastroenterology & Urology · 148d

Cleared Jan 22, 1988

DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODE

URDYN 5000 (UROFLOWMETER)

K860368 · FFO

Gastroenterology & Urology · 79d

Cleared Oct 04, 1985

URODYN 1000

K853119 · FFO

Gastroenterology & Urology · 71d

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

FDA 510(k) cleared devices by Dantec Electronics, Inc.

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