Skin Clinic Nitro Clear Wart Remover
K-Number: K242932 · 2025-04-15
Device Summary
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. The listed applicant is Cryoconcepts LP. The 510(k) number is K242932.
When did Skin Clinic Nitro Clear Wart Remover receive FDA 510(k) clearance?
Skin Clinic Nitro Clear Wart Remover received FDA 510(k) clearance on 2025-04-15, under 510(k) number K242932.
Who is the listed applicant for Skin Clinic Nitro Clear Wart Remover?
The FDA 510(k) record lists Cryoconcepts LP as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Cryoconcepts LP as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GEH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.