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FDA 510(k)

Compound W Wart Removal System Dual Power

K-Number: K161294 · 2016-09-15

ApplicantMedtech Products, Inc.
Decision Date2016-09-15
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Compound W Wart Removal System Dual Power is a medical device manufactured by Medtech Products, Inc.. It received FDA 510(k) clearance on 2016-09-15 under approval number K161294. 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 Compound W Wart Removal System Dual Power?

Compound W Wart Removal System Dual Power is a medical device that received FDA 510(k) clearance on 2016-09-15. It is manufactured by Medtech Products, Inc.. The 510(k) number is K161294.

When was Compound W Wart Removal System Dual Power approved by the FDA?

Compound W Wart Removal System Dual Power received FDA 510(k) clearance on 2016-09-15, under approval number K161294.

What company makes Compound W Wart Removal System Dual Power?

Compound W Wart Removal System Dual Power is manufactured by Medtech Products, Inc..

What is the FDA product code for Compound W Wart Removal System Dual Power?

The FDA product code for Compound W Wart Removal System Dual Power is GEH.

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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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