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FDA 510(k)

FIBREX CATHETER PATENCY DEVICE

K-Number: K040427 · 2004-05-03

ApplicantMedical Device Technologies, Inc.
Decision Date2004-05-03
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FIBREX CATHETER PATENCY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2004-05-03 under 510(k) number K040427. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBREX CATHETER PATENCY DEVICE?

FIBREX CATHETER PATENCY DEVICE is a medical device that received FDA 510(k) clearance on 2004-05-03. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K040427.

When did FIBREX CATHETER PATENCY DEVICE receive FDA 510(k) clearance?

FIBREX CATHETER PATENCY DEVICE received FDA 510(k) clearance on 2004-05-03, under 510(k) number K040427.

Who is the listed applicant for FIBREX CATHETER PATENCY DEVICE?

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

What is the FDA product code for FIBREX CATHETER PATENCY DEVICE?

The FDA product code for FIBREX CATHETER PATENCY DEVICE is FOZ.

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Related Devices (Code: FOZ)

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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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