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FDA 510(k)

DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2)

K-Number: K902607 · 1991-05-14

ApplicantDantec Medical, Inc.
Decision Date1991-05-14
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2) is the device name listed in this FDA 510(k) record. The listed applicant is Dantec Medical, Inc.. It received FDA 510(k) clearance on 1991-05-14 under 510(k) number K902607. 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 MAG 2 (MAG 2)?

DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2) is a medical device that received FDA 510(k) clearance on 1991-05-14. The listed applicant is Dantec Medical, Inc.. The 510(k) number is K902607.

When did DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2) receive FDA 510(k) clearance?

DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2) received FDA 510(k) clearance on 1991-05-14, under 510(k) number K902607.

Who is the listed applicant for DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2)?

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

What is the FDA product code for DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2)?

The FDA product code for DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2) is GWF.

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Other records listing Dantec Medical, 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.

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Related Devices (Code: GWF)

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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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