Dantec Medical, Inc.
Dantec Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1996.
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.