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FDA 510(k)

FORCE FIBER

K-Number: K033654 · 2004-01-15

ApplicantTeleflex Medical
Decision Date2004-01-15
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCE FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2004-01-15 under 510(k) number K033654. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCE FIBER?

FORCE FIBER is a medical device that received FDA 510(k) clearance on 2004-01-15. The listed applicant is Teleflex Medical. The 510(k) number is K033654.

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

FORCE FIBER received FDA 510(k) clearance on 2004-01-15, under 510(k) number K033654.

Who is the listed applicant for FORCE FIBER?

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

What is the FDA product code for FORCE FIBER?

The FDA product code for FORCE FIBER is GAT.

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Other records listing Teleflex Medical as applicant

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Related Devices (Code: GAT)

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K253910Stitch - Suture Wires and TapesGM Dos Reis Industria e Comercio Ltda.K261021EasyWhip FamilyWinter Innovations, Inc.K260775Polyethylene;Polyethylene Fusion;Polyethylene OrthoTape™Teleflex Medical, LLCK254275HyperSuture All Green Extension LineThreadstone, LLCK254188Meniscus VersaflexGM Dos Reis Industria e Comercio Ltda.K253145Pre-Sutured TendonRti Surgical, Inc.

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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