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FDA 510(k)

VERSACATH SELECTALUMEN INNER CATHETER

K-Number: K920133 · 1992-03-26

ApplicantMenlo Care, Inc.
Decision Date1992-03-26
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERSACATH SELECTALUMEN INNER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Menlo Care, Inc.. It received FDA 510(k) clearance on 1992-03-26 under 510(k) number K920133. 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 VERSACATH SELECTALUMEN INNER CATHETER?

VERSACATH SELECTALUMEN INNER CATHETER is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Menlo Care, Inc.. The 510(k) number is K920133.

When did VERSACATH SELECTALUMEN INNER CATHETER receive FDA 510(k) clearance?

VERSACATH SELECTALUMEN INNER CATHETER received FDA 510(k) clearance on 1992-03-26, under 510(k) number K920133.

Who is the listed applicant for VERSACATH SELECTALUMEN INNER CATHETER?

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

What is the FDA product code for VERSACATH SELECTALUMEN INNER CATHETER?

The FDA product code for VERSACATH SELECTALUMEN INNER CATHETER is FOZ.

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Other records listing Menlo Care, Inc. as applicant

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Related Devices (Code: 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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