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FDA 510(k)

VERSACATH(TM) MULTILUMEN SYSTEM

K-Number: K910566 · 1991-06-03

ApplicantMenlo Care, Inc.
Decision Date1991-06-03
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

VERSACATH(TM) MULTILUMEN SYSTEM 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 1991-06-03 under 510(k) number K910566. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VERSACATH(TM) MULTILUMEN SYSTEM?

VERSACATH(TM) MULTILUMEN SYSTEM is a medical device that received FDA 510(k) clearance on 1991-06-03. The listed applicant is Menlo Care, Inc.. The 510(k) number is K910566.

When did VERSACATH(TM) MULTILUMEN SYSTEM receive FDA 510(k) clearance?

VERSACATH(TM) MULTILUMEN SYSTEM received FDA 510(k) clearance on 1991-06-03, under 510(k) number K910566.

Who is the listed applicant for VERSACATH(TM) MULTILUMEN SYSTEM?

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(TM) MULTILUMEN SYSTEM?

The FDA product code for VERSACATH(TM) MULTILUMEN SYSTEM 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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