FDA 510(k)

Novilase Laser Therapy System, Model LTS-2

K-번호: K160392 · 2016-02-26

결정일2016-02-26

제품 코드GEX

자문 위원회SU

결정Substantially Equivalent

기기 요약

Novilase Laser Therapy System, Model LTS-2 is the device name listed in this FDA 510(k) record. The listed applicant is Novian Health, Inc.. It received FDA 510(k) clearance on 2016-02-26 under 510(k) number K160392. 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 Novilase Laser Therapy System, Model LTS-2?

Novilase Laser Therapy System, Model LTS-2 is a medical device that received FDA 510(k) clearance on 2016-02-26. The listed applicant is Novian Health, Inc.. The 510(k) number is K160392.

When did Novilase Laser Therapy System, Model LTS-2 receive FDA 510(k) clearance?

Novilase Laser Therapy System, Model LTS-2 received FDA 510(k) clearance on 2016-02-26, under 510(k) number K160392.

Who is the listed applicant for Novilase Laser Therapy System, Model LTS-2?

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

What is the FDA product code for Novilase Laser Therapy System, Model LTS-2?

The FDA product code for Novilase Laser Therapy System, Model LTS-2 is GEX. This falls under the Gastroenterology category.

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Novilase Laser Therapy System, Model LTS-2

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: GEX)

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