FDA 510(k)

AcuPulse (früher AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO

K-Nummer: K180597 · 2018-04-03

Entscheidungsdatum2018-04-03

ProduktcodeGEX

BeratungsausschussSU

EntscheidungSubstantially Equivalent

Produktübersicht

AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO is the device name listed in this FDA 510(k) record. The listed applicant is Lumenis, Ltd.. It received FDA 510(k) clearance on 2018-04-03 under 510(k) number K180597. 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.

Häufig gestellte Fragen

What is the AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO?

AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO is a medical device that received FDA 510(k) clearance on 2018-04-03. The listed applicant is Lumenis, Ltd.. The 510(k) number is K180597.

When did AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO receive FDA 510(k) clearance?

AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO received FDA 510(k) clearance on 2018-04-03, under 510(k) number K180597.

Who is the listed applicant for AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO?

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

What is the FDA product code for AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO?

The FDA product code for AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO is GEX. This falls under the Gastroenterology category.

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