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FDA 510(k)

OPTILITE FIBEROPTIC DELIVERY SYSTEMS

K-Number: K902871 · 1990-09-24

ApplicantXintec Corporation
Decision Date1990-09-24
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPTILITE FIBEROPTIC DELIVERY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Xintec Corporation. It received FDA 510(k) clearance on 1990-09-24 under 510(k) number K902871. 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 OPTILITE FIBEROPTIC DELIVERY SYSTEMS?

OPTILITE FIBEROPTIC DELIVERY SYSTEMS is a medical device that received FDA 510(k) clearance on 1990-09-24. The listed applicant is Xintec Corporation. The 510(k) number is K902871.

When did OPTILITE FIBEROPTIC DELIVERY SYSTEMS receive FDA 510(k) clearance?

OPTILITE FIBEROPTIC DELIVERY SYSTEMS received FDA 510(k) clearance on 1990-09-24, under 510(k) number K902871.

Who is the listed applicant for OPTILITE FIBEROPTIC DELIVERY SYSTEMS?

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

What is the FDA product code for OPTILITE FIBEROPTIC DELIVERY SYSTEMS?

The FDA product code for OPTILITE FIBEROPTIC DELIVERY SYSTEMS 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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