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.

Dantec Electronics, 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 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) Regulatory Record - Dantec Electronics, Inc.

Filters