FDA 510(k)

Merlexi Craft Bariatric series of manual wheelchairs

K-번호: K240120 · 2024-07-05

결정일2024-07-05

제품 코드IOR

자문 위원회PM

결정Substantially Equivalent

기기 요약

Merlexi Craft Bariatric series of manual wheelchairs is the device name listed in this FDA 510(k) record. The listed applicant is Turbo Wheelchair Co., Inc.. It received FDA 510(k) clearance on 2024-07-05 under 510(k) number K240120. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Merlexi Craft Bariatric series of manual wheelchairs?

Merlexi Craft Bariatric series of manual wheelchairs is a medical device that received FDA 510(k) clearance on 2024-07-05. The listed applicant is Turbo Wheelchair Co., Inc.. The 510(k) number is K240120.

When did Merlexi Craft Bariatric series of manual wheelchairs receive FDA 510(k) clearance?

Merlexi Craft Bariatric series of manual wheelchairs received FDA 510(k) clearance on 2024-07-05, under 510(k) number K240120.

Who is the listed applicant for Merlexi Craft Bariatric series of manual wheelchairs?

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

What is the FDA product code for Merlexi Craft Bariatric series of manual wheelchairs?

The FDA product code for Merlexi Craft Bariatric series of manual wheelchairs is IOR.

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Merlexi Craft Bariatric series of manual wheelchairs

기기 요약

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관련 임상시험

관련 기기 (코드: IOR)

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