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FDA 510(k)

BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55

K-Number: K130197 · 2013-02-27

Decision Date2013-02-27
Product CodeONB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55 is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2013-02-27 under 510(k) number K130197. The device is classified under product code ONB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55?

BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55 is a medical device that received FDA 510(k) clearance on 2013-02-27. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K130197.

When did BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55 receive FDA 510(k) clearance?

BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55 received FDA 510(k) clearance on 2013-02-27, under 510(k) number K130197.

Who is the listed applicant for BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55?

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

What is the FDA product code for BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55?

The FDA product code for BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55 is ONB.

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 and Company 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.

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Related Devices (Code: ONB)

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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