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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 the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2016-09-15 under 510(k) 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. The listed applicant is Medtech Products, Inc.. The 510(k) number is K161294.

When did Compound W Wart Removal System Dual Power receive FDA 510(k) clearance?

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

Who is the listed applicant for Compound W Wart Removal System Dual Power?

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

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.

Other records listing Medtech Products, Inc. as applicant

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Official Source

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