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FDA 510(k)

BD POSIFLOW POSITIVE DISPLACEMENT VALVE

K-Number: K050207 · 2005-04-07

Decision Date2005-04-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD POSIFLOW POSITIVE DISPLACEMENT VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2005-04-07 under 510(k) number K050207. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD POSIFLOW POSITIVE DISPLACEMENT VALVE?

BD POSIFLOW POSITIVE DISPLACEMENT VALVE is a medical device that received FDA 510(k) clearance on 2005-04-07. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K050207.

When did BD POSIFLOW POSITIVE DISPLACEMENT VALVE receive FDA 510(k) clearance?

BD POSIFLOW POSITIVE DISPLACEMENT VALVE received FDA 510(k) clearance on 2005-04-07, under 510(k) number K050207.

Who is the listed applicant for BD POSIFLOW POSITIVE DISPLACEMENT VALVE?

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

What is the FDA product code for BD POSIFLOW POSITIVE DISPLACEMENT VALVE?

The FDA product code for BD POSIFLOW POSITIVE DISPLACEMENT VALVE is FPA.

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 Becton Dickinson Infusion Therapy Systems, 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.

View all 34 devices →

Related Devices (Code: FPA)

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

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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