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FDA 510(k)

E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET

K-Number: K970259 · 1997-04-08

Decision Date1997-04-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET 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 1997-04-08 under 510(k) number K970259. 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 E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET?

E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET is a medical device that received FDA 510(k) clearance on 1997-04-08. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K970259.

When did E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET receive FDA 510(k) clearance?

E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET received FDA 510(k) clearance on 1997-04-08, under 510(k) number K970259.

Who is the listed applicant for E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET?

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 E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET?

The FDA product code for E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET 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 Vascular Access, 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 25 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

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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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