FDA 510(k)

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K-번호: K233224 · 2024-01-27

신청자Epilady 2000, LLC

결정일2024-01-27

제품 코드GEX

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

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기기 요약

Epilaser Pro is the device name listed in this FDA 510(k) record. The listed applicant is Epilady 2000, LLC. It received FDA 510(k) clearance on 2024-01-27 under 510(k) number K233224. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Epilaser Pro?

Epilaser Pro is a medical device that received FDA 510(k) clearance on 2024-01-27. The listed applicant is Epilady 2000, LLC. The 510(k) number is K233224.

When did Epilaser Pro receive FDA 510(k) clearance?

Epilaser Pro received FDA 510(k) clearance on 2024-01-27, under 510(k) number K233224.

Who is the listed applicant for Epilaser Pro?

The FDA 510(k) record lists Epilady 2000, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Epilaser Pro?

The FDA product code for Epilaser Pro is GEX. This falls under the Gastroenterology category.

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