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FDA 510(k)

Skin Clinic Nitro Clear Wart Remover

K-Number: K242932 · 2025-04-15

ApplicantCryoconcepts LP
Decision Date2025-04-15
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Skin Clinic Nitro Clear Wart Remover is a medical device manufactured by Cryoconcepts LP. It received FDA 510(k) clearance on 2025-04-15 under approval number K242932. 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 Skin Clinic Nitro Clear Wart Remover?

Skin Clinic Nitro Clear Wart Remover is a medical device that received FDA 510(k) clearance on 2025-04-15. It is manufactured by Cryoconcepts LP. The 510(k) number is K242932.

When was Skin Clinic Nitro Clear Wart Remover approved by the FDA?

Skin Clinic Nitro Clear Wart Remover received FDA 510(k) clearance on 2025-04-15, under approval number K242932.

What company makes Skin Clinic Nitro Clear Wart Remover?

Skin Clinic Nitro Clear Wart Remover is manufactured by Cryoconcepts LP.

What is the FDA product code for Skin Clinic Nitro Clear Wart Remover?

The FDA product code for Skin Clinic Nitro Clear Wart Remover 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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