FDA 510(k)

SLI Endoprobe, SLI DENT Klarfaser, SLI HO Klarfaser, SLI HCS Klarfaser, SLI Längsfeuer Klarfaser

K-Nummer: K151855 · 2016-04-15

AntragstellerSurgical Laser Incorporated

Entscheidungsdatum2016-04-15

ProduktcodeGEX

BeratungsausschussSU I'm sorry, but it seems like the text you provided is incomplete. Could you please provide the full description or text that you would like translated into German?

EntscheidungSubstantiell Äquivalent

Produktübersicht

SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Laser Incorporated. It received FDA 510(k) clearance on 2016-04-15 under 510(k) number K151855. 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 SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber?

SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber is a medical device that received FDA 510(k) clearance on 2016-04-15. The listed applicant is Surgical Laser Incorporated. The 510(k) number is K151855.

When did SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber receive FDA 510(k) clearance?

SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber received FDA 510(k) clearance on 2016-04-15, under 510(k) number K151855.

Who is the listed applicant for SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber?

The FDA 510(k) record lists Surgical Laser Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber?

The FDA product code for SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber is GEX. This falls under the Gastroenterology category.

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