FDA 510(k)

OGYILI TENS/NMES Stimulator

K-번호: K201431 · 2020-11-09

결정일2020-11-09

제품 코드GZJ

자문 위원회NE

결정Substantially Equivalent

기기 요약

OGYILI TENS/NMES Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Gongguan Tutamen Metalwork Co., Ltd.. It received FDA 510(k) clearance on 2020-11-09 under 510(k) number K201431. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the OGYILI TENS/NMES Stimulator?

OGYILI TENS/NMES Stimulator is a medical device that received FDA 510(k) clearance on 2020-11-09. The listed applicant is Gongguan Tutamen Metalwork Co., Ltd.. The 510(k) number is K201431.

When did OGYILI TENS/NMES Stimulator receive FDA 510(k) clearance?

OGYILI TENS/NMES Stimulator received FDA 510(k) clearance on 2020-11-09, under 510(k) number K201431.

Who is the listed applicant for OGYILI TENS/NMES Stimulator?

The FDA 510(k) record lists Gongguan Tutamen Metalwork Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OGYILI TENS/NMES Stimulator?

The FDA product code for OGYILI TENS/NMES Stimulator is GZJ.

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OGYILI TENS/NMES Stimulator

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: GZJ)

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