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FDA 510(k)

NOVACATH SECURE IV CATHETER SYSTEM-18G

K-Number: K120839 · 2012-07-20

Decision Date2012-07-20
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVACATH SECURE IV CATHETER SYSTEM-18G is the device name listed in this FDA 510(k) record. The listed applicant is Tangent Medical Technologies, Inc.. It received FDA 510(k) clearance on 2012-07-20 under 510(k) number K120839. 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 NOVACATH SECURE IV CATHETER SYSTEM-18G?

NOVACATH SECURE IV CATHETER SYSTEM-18G is a medical device that received FDA 510(k) clearance on 2012-07-20. The listed applicant is Tangent Medical Technologies, Inc.. The 510(k) number is K120839.

When did NOVACATH SECURE IV CATHETER SYSTEM-18G receive FDA 510(k) clearance?

NOVACATH SECURE IV CATHETER SYSTEM-18G received FDA 510(k) clearance on 2012-07-20, under 510(k) number K120839.

Who is the listed applicant for NOVACATH SECURE IV CATHETER SYSTEM-18G?

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

What is the FDA product code for NOVACATH SECURE IV CATHETER SYSTEM-18G?

The FDA product code for NOVACATH SECURE IV CATHETER SYSTEM-18G is FOZ.

Related Clinical Trials

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.

Other records listing Tangent Medical Technologies, Inc. as applicant

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.

Related Devices (Code: FOZ)

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.

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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