ClearanceBrief
Company ยท US

Dantec Electronics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1990. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GWFStimulator, Electrical, Evoked Response4
FAPCystometric Gas (Carbon-Dioxide) On Hydraulic Device3
FFORetractor, Self-Retaining2
GXYElectrode, Cutaneous1
GXZElectrode, Needle1
IKTElectrode, Needle, Diagnostic Electromyograph1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 18, 1990K895460CONCENTRIC ELECTRODE TYPE #13R01, 13R02
Dantec Electronics, Inc.
IKT
May 14, 1990K894911SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118
Dantec Electronics, Inc.
GXZ
Oct 4, 1989K884915DANTEC 22K60/61/62 CATHETER TIP TRANSDUCER
Dantec Electronics, Inc.
FAP
Oct 17, 1988K881915DANTEC MAGNETIC STIMULATOR
Dantec Electronics, Inc.
GWF
Apr 14, 1988K87475913L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLE
Dantec Electronics, Inc.
FAP
Apr 14, 1988K874758DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE
Dantec Electronics, Inc.
FAP
Jan 22, 1988K874735DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODE
Dantec Electronics, Inc.
GXY
Oct 6, 1987K870567EVOPORT 300
Dantec Electronics, Inc.
GWF
Sep 10, 1987K872106DANTEC COUNTERPOINT
Dantec Electronics, Inc.
GWF
Apr 23, 1986K860368URDYN 5000 (UROFLOWMETER)
Dantec Electronics, Inc.
FFO
Oct 4, 1985K853119URODYN 1000
Dantec Electronics, Inc.
FFO
May 31, 1985K843815EVOMATIC 8000/4000
Dantec Electronics, Inc.
GWF

Latest recalls

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