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FDA 510(k)

DANTEC MAGNETIC STIMULATOR

K-Number: K881915 · 1988-10-17

ApplicantDantec Electronics, Inc.
Decision Date1988-10-17
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DANTEC MAGNETIC STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dantec Electronics, Inc.. It received FDA 510(k) clearance on 1988-10-17 under 510(k) number K881915. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANTEC MAGNETIC STIMULATOR?

DANTEC MAGNETIC STIMULATOR is a medical device that received FDA 510(k) clearance on 1988-10-17. The listed applicant is Dantec Electronics, Inc.. The 510(k) number is K881915.

When did DANTEC MAGNETIC STIMULATOR receive FDA 510(k) clearance?

DANTEC MAGNETIC STIMULATOR received FDA 510(k) clearance on 1988-10-17, under 510(k) number K881915.

Who is the listed applicant for DANTEC MAGNETIC STIMULATOR?

The FDA 510(k) record lists Dantec Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DANTEC MAGNETIC STIMULATOR?

The FDA product code for DANTEC MAGNETIC STIMULATOR is GWF.

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Other records listing Dantec Electronics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K895460CONCENTRIC ELECTRODE TYPE #13R01, 13R02K894911SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118K884915DANTEC 22K60/61/62 CATHETER TIP TRANSDUCERK874758DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODEK87475913L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLEK874735DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODE

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Related Devices (Code: GWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K263010ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpressinomed Medizintechnik GmbHK253301BraiN20® (BraiN20)Time IS Brain, S.L.K252842SafeOp 3: Neural Informatix SystemAlphatec Spine, Inc.K243982Nicolet EDXNatus Neurology IncorporatedK243495Natus Ultrapro S100 (982A0594)Natus Neurology IncorporatedK242345Delphi StimulatorQuantalx Neuroscience

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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