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FDA 510(k)

UFR FIBEROPTIC CABLE

K-Number: K972225 · 1998-03-18

ApplicantUniversal Fiberoptic Repair, Inc.
Decision Date1998-03-18
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UFR FIBEROPTIC CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Universal Fiberoptic Repair, Inc.. It received FDA 510(k) clearance on 1998-03-18 under 510(k) number K972225. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UFR FIBEROPTIC CABLE?

UFR FIBEROPTIC CABLE is a medical device that received FDA 510(k) clearance on 1998-03-18. The listed applicant is Universal Fiberoptic Repair, Inc.. The 510(k) number is K972225.

When did UFR FIBEROPTIC CABLE receive FDA 510(k) clearance?

UFR FIBEROPTIC CABLE received FDA 510(k) clearance on 1998-03-18, under 510(k) number K972225.

Who is the listed applicant for UFR FIBEROPTIC CABLE?

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

What is the FDA product code for UFR FIBEROPTIC CABLE?

The FDA product code for UFR FIBEROPTIC CABLE is FST.

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Related Devices (Code: FST)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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