Dantec Electronics, Inc.
Dantec Electronics, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1990.
Top product codes for Dantec Electronics, Inc.
Recent clearances by Dantec Electronics, Inc.
- K895460 — CONCENTRIC ELECTRODE TYPE #13R01, 13R02
- K894911 — SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118
- K884915 — DANTEC 22K60/61/62 CATHETER TIP TRANSDUCER
- K881915 — DANTEC MAGNETIC STIMULATOR
- K874758 — DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE
- K874759 — 13L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLE
- K874735 — DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODE
- K870567 — EVOPORT 300
- K872106 — DANTEC COUNTERPOINT
- K860368 — URDYN 5000 (UROFLOWMETER)
- K853119 — URODYN 1000
- K843815 — EVOMATIC 8000/4000
Data sourced from openFDA. This site is unofficial and independent of the FDA.