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FDA 510(k)

MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122

K-Number: K040228 · 2004-04-29

ApplicantMedi-Stim A/S
Decision Date2004-04-29
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Stim A/S. It received FDA 510(k) clearance on 2004-04-29 under 510(k) number K040228. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122?

MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 is a medical device that received FDA 510(k) clearance on 2004-04-29. The listed applicant is Medi-Stim A/S. The 510(k) number is K040228.

When did MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 receive FDA 510(k) clearance?

MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 received FDA 510(k) clearance on 2004-04-29, under 510(k) number K040228.

Who is the listed applicant for MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122?

The FDA 510(k) record lists Medi-Stim A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122?

The FDA product code for MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 is DPW.

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Other records listing Medi-Stim A/S 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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Official Source

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