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FDA 510(k)

E-Z SET/MINICATH INFUSION SETS

K-Number: K920635 · 1992-04-06

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-04-06
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E-Z SET/MINICATH INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1992-04-06 under 510(k) number K920635. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-Z SET/MINICATH INFUSION SETS?

E-Z SET/MINICATH INFUSION SETS is a medical device that received FDA 510(k) clearance on 1992-04-06. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K920635.

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

E-Z SET/MINICATH INFUSION SETS received FDA 510(k) clearance on 1992-04-06, under 510(k) number K920635.

Who is the listed applicant for E-Z SET/MINICATH INFUSION SETS?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-Z SET/MINICATH INFUSION SETS?

The FDA product code for E-Z SET/MINICATH INFUSION SETS is FOZ.

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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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