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FDA 510(k)

VARI-LASE WIRE FIBER

K-Number: K072332 · 2008-01-10

ApplicantVascular Solutions, Inc.
Decision Date2008-01-10
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VARI-LASE WIRE FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2008-01-10 under 510(k) number K072332. 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.

Frequently Asked Questions

What is the VARI-LASE WIRE FIBER?

VARI-LASE WIRE FIBER is a medical device that received FDA 510(k) clearance on 2008-01-10. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K072332.

When did VARI-LASE WIRE FIBER receive FDA 510(k) clearance?

VARI-LASE WIRE FIBER received FDA 510(k) clearance on 2008-01-10, under 510(k) number K072332.

Who is the listed applicant for VARI-LASE WIRE FIBER?

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

What is the FDA product code for VARI-LASE WIRE FIBER?

The FDA product code for VARI-LASE WIRE FIBER is GEX. This falls under the Gastroenterology category.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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