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FDA 510(k)

MEDISTIM VERIQC SYSTEM

K-Number: K102595 · 2010-12-27

ApplicantMedi-Stim Asa
Decision Date2010-12-27
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDISTIM VERIQC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Stim Asa. It received FDA 510(k) clearance on 2010-12-27 under 510(k) number K102595. 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 MEDISTIM VERIQC SYSTEM?

MEDISTIM VERIQC SYSTEM is a medical device that received FDA 510(k) clearance on 2010-12-27. The listed applicant is Medi-Stim Asa. The 510(k) number is K102595.

When did MEDISTIM VERIQC SYSTEM receive FDA 510(k) clearance?

MEDISTIM VERIQC SYSTEM received FDA 510(k) clearance on 2010-12-27, under 510(k) number K102595.

Who is the listed applicant for MEDISTIM VERIQC SYSTEM?

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

What is the FDA product code for MEDISTIM VERIQC SYSTEM?

The FDA product code for MEDISTIM VERIQC SYSTEM is DPW.

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Official Source

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