FDA 510(k)

E-Z SET(R) AND MINICATH(R) INFUSION SETS

K-Number: K950302 · 1995-03-13

ApplicantBecton Dickinson Vascular Access, Inc.

Decision Date1995-03-13

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

E-Z SET(R) AND MINICATH(R) INFUSION SETS 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 1995-03-13 under 510(k) number K950302. 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(R) AND MINICATH(R) INFUSION SETS?

E-Z SET(R) AND MINICATH(R) INFUSION SETS is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K950302.

When did E-Z SET(R) AND MINICATH(R) INFUSION SETS receive FDA 510(k) clearance?

E-Z SET(R) AND MINICATH(R) INFUSION SETS received FDA 510(k) clearance on 1995-03-13, under 510(k) number K950302.

Who is the listed applicant for E-Z SET(R) AND MINICATH(R) INFUSION SETS?

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(R) AND MINICATH(R) INFUSION SETS?

The FDA product code for E-Z SET(R) AND MINICATH(R) INFUSION SETS is FPA.

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

K971339INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERS K970259E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET K964049FIRST MIDCATH CATHETER WITH DUAL LUMENS K964050FIRST MIDCATH CATHETER K964048FIRST MIDCATH CATHETER KIT K954906FIRST PICC INTRODUCER CATHETER

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Related Devices (Code: FPA)

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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.