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FDA 510(k)

THE FLEX-SET SUBCUTANEOUS INFUSION SET

K-Number: K944302 · 1995-04-10

ApplicantCathco, Inc.
Decision Date1995-04-10
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE FLEX-SET SUBCUTANEOUS INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Cathco, Inc.. It received FDA 510(k) clearance on 1995-04-10 under 510(k) number K944302. 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 THE FLEX-SET SUBCUTANEOUS INFUSION SET?

THE FLEX-SET SUBCUTANEOUS INFUSION SET is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Cathco, Inc.. The 510(k) number is K944302.

When did THE FLEX-SET SUBCUTANEOUS INFUSION SET receive FDA 510(k) clearance?

THE FLEX-SET SUBCUTANEOUS INFUSION SET received FDA 510(k) clearance on 1995-04-10, under 510(k) number K944302.

Who is the listed applicant for THE FLEX-SET SUBCUTANEOUS INFUSION SET?

The FDA 510(k) record lists Cathco, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE FLEX-SET SUBCUTANEOUS INFUSION SET?

The FDA product code for THE FLEX-SET SUBCUTANEOUS INFUSION SET is FOZ.

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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.

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