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FDA 510(k)

DESERET(R) FLOW RESTRICTION VALVE

K-Number: K914180 · 1992-05-08

ApplicantBecton Dickinson Vascular Access, Inc.
Decision Date1992-05-08
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

DESERET(R) FLOW RESTRICTION VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vascular Access, Inc.. It received FDA 510(k) clearance on 1992-05-08 under 510(k) number K914180. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DESERET(R) FLOW RESTRICTION VALVE?

DESERET(R) FLOW RESTRICTION VALVE is a medical device that received FDA 510(k) clearance on 1992-05-08. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K914180.

When did DESERET(R) FLOW RESTRICTION VALVE receive FDA 510(k) clearance?

DESERET(R) FLOW RESTRICTION VALVE received FDA 510(k) clearance on 1992-05-08, under 510(k) number K914180.

Who is the listed applicant for DESERET(R) FLOW RESTRICTION VALVE?

The FDA 510(k) record lists Becton Dickinson Vascular Access, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET(R) FLOW RESTRICTION VALVE?

The FDA product code for DESERET(R) FLOW RESTRICTION VALVE is FOZ.

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Other records listing Becton Dickinson Vascular Access, Inc. as applicant

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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.

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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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