FDA 510(k)

dS Small Extremity 16CH 1.5T Coil

K-번호: K162863 · 2016-11-07

결정일2016-11-07

제품 코드MOS

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

결정대체적으로 동일

기기 요약

dS Small Extremity 16CH 1.5T Coil is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Therapeutics Corporation. It received FDA 510(k) clearance on 2016-11-07 under 510(k) number K162863. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the dS Small Extremity 16CH 1.5T Coil?

dS Small Extremity 16CH 1.5T Coil is a medical device that received FDA 510(k) clearance on 2016-11-07. The listed applicant is Invivo Therapeutics Corporation. The 510(k) number is K162863.

When did dS Small Extremity 16CH 1.5T Coil receive FDA 510(k) clearance?

dS Small Extremity 16CH 1.5T Coil received FDA 510(k) clearance on 2016-11-07, under 510(k) number K162863.

Who is the listed applicant for dS Small Extremity 16CH 1.5T Coil?

The FDA 510(k) record lists Invivo Therapeutics Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for dS Small Extremity 16CH 1.5T Coil?

The FDA product code for dS Small Extremity 16CH 1.5T Coil is MOS.

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dS Small Extremity 16CH 1.5T Coil

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: MOS)

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