FDA 510(k)

Neuromuscular Transmission Monitor TOF3D (2510091)

K-번호: K250887 · 2025-10-21

신청자MIPM Mammendorfer Institut für Physik und Medizin GmbH

결정일2025-10-21

제품 코드KOI

자문 위원회AN

결정Substantially Equivalent

기기 요약

Neuromuscular Transmission Monitor TOF3D (2510091) is the device name listed in this FDA 510(k) record. The listed applicant is MIPM Mammendorfer Institut für Physik und Medizin GmbH. It received FDA 510(k) clearance on 2025-10-21 under 510(k) number K250887. The device is classified under product code KOI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Neuromuscular Transmission Monitor TOF3D (2510091)?

Neuromuscular Transmission Monitor TOF3D (2510091) is a medical device that received FDA 510(k) clearance on 2025-10-21. The listed applicant is MIPM Mammendorfer Institut für Physik und Medizin GmbH. The 510(k) number is K250887.

When did Neuromuscular Transmission Monitor TOF3D (2510091) receive FDA 510(k) clearance?

Neuromuscular Transmission Monitor TOF3D (2510091) received FDA 510(k) clearance on 2025-10-21, under 510(k) number K250887.

Who is the listed applicant for Neuromuscular Transmission Monitor TOF3D (2510091)?

The FDA 510(k) record lists MIPM Mammendorfer Institut für Physik und Medizin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Neuromuscular Transmission Monitor TOF3D (2510091)?

The FDA product code for Neuromuscular Transmission Monitor TOF3D (2510091) is KOI.

MIPM Mammendorfer Institut für Physik und Medizin GmbH를 신청인으로 등재한 기타 기록

K212434Neuromuscular Transmission Monitor TOF3D

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