Dantec Medical, Inc.
FDA 510(k) medical device clearances.
Top product codes for Dantec Medical, Inc.
Recent clearances by Dantec Medical, Inc.
- K960503 — DANTEC DUET
- K950314 — DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)
- K953999 — DANTEC DA CAPO
- K926363 — MULTI-DOP S
- K931801 — MULTI-DOP X
- K930458 — MULTI-DOP L
- K932059 — NEEDLE ELECTRODES AND DISPOSABLE SCALP ELECTRODE
- K934580 — DANTEC 13R45 BAR ELECTRODE
- K931966 — DANTEC DISPOSABLE CONCENTRIC NEEDLE
- K931923 — DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE)
- K926516 — DANTEC MAGNETIC STIMULATOR MAGPRO
- K924127 — DANTEC EVOLUTION
- K923117 — CAVERNOSOMETRY MODULE FOR MENUET
- K915741 — DISPOSABLE MONOPLAR MEDDLE ELECTRODES
- K913957 — DANTEC COUNTERPOINT MK2(TM)
- K913169 — DANTEC UD 5500 MK2
- K914891 — PULLER OPTION FOR ETUDE(TM)
- K912701 — DANTEC MENUET
- K911229 — PHOENIX DIGITAL EEG SYSTEM
- K913323 — ETUDE (MODEL NUMBERS 24A05 & 24A06)
- K902607 — DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2)
- K901494 — ETUDE, URODYNAMIC INVESTIGATION SYSTEM
- K896874 — DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12
- K896575 — DANTEC MENUET
- K896567 — CANTATA EMG/EVOKED RESPONSE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.