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FDA 510(k)

WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)

K-Number: K032271 · 2003-09-10

ApplicantWartner USA B.V.
Decision Date2003-09-10
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) is the device name listed in this FDA 510(k) record. The listed applicant is Wartner USA B.V.. It received FDA 510(k) clearance on 2003-09-10 under 510(k) number K032271. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)?

WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) is a medical device that received FDA 510(k) clearance on 2003-09-10. The listed applicant is Wartner USA B.V.. The 510(k) number is K032271.

When did WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) receive FDA 510(k) clearance?

WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) received FDA 510(k) clearance on 2003-09-10, under 510(k) number K032271.

Who is the listed applicant for WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)?

The FDA 510(k) record lists Wartner USA B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)?

The FDA product code for WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) is GEH.

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Official Source

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

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