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FDA 510(k)

MENLO CARE AQUASTENT SET

K-Number: K923394 · 1993-11-16

ApplicantMenlo Care, Inc.
Decision Date1993-11-16
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MENLO CARE AQUASTENT SET 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 1993-11-16 under 510(k) number K923394. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENLO CARE AQUASTENT SET?

MENLO CARE AQUASTENT SET is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Menlo Care, Inc.. The 510(k) number is K923394.

When did MENLO CARE AQUASTENT SET receive FDA 510(k) clearance?

MENLO CARE AQUASTENT SET received FDA 510(k) clearance on 1993-11-16, under 510(k) number K923394.

Who is the listed applicant for MENLO CARE AQUASTENT SET?

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 MENLO CARE AQUASTENT SET?

The FDA product code for MENLO CARE AQUASTENT SET is FAD.

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Related Devices (Code: FAD)

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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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