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FDA 510(k)

FIBER MESH

K-Number: K855005 · 1986-01-30

ApplicantFiber Mesh, Inc.
Decision Date1986-01-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER MESH is the device name listed in this FDA 510(k) record. The listed applicant is Fiber Mesh, Inc.. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K855005. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER MESH?

FIBER MESH is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Fiber Mesh, Inc.. The 510(k) number is K855005.

When did FIBER MESH receive FDA 510(k) clearance?

FIBER MESH received FDA 510(k) clearance on 1986-01-30, under 510(k) number K855005.

Who is the listed applicant for FIBER MESH?

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

What is the FDA product code for FIBER MESH?

The FDA product code for FIBER MESH is DZE.

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Related Devices (Code: DZE)

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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