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FDA 510(k)

AUGUSTA VALENTINI

K-Number: K923884 · 1993-03-18

ApplicantRevue Intl.
Decision Date1993-03-18
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUGUSTA VALENTINI is the device name listed in this FDA 510(k) record. The listed applicant is Revue Intl.. It received FDA 510(k) clearance on 1993-03-18 under 510(k) number K923884. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUGUSTA VALENTINI?

AUGUSTA VALENTINI is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Revue Intl.. The 510(k) number is K923884.

When did AUGUSTA VALENTINI receive FDA 510(k) clearance?

AUGUSTA VALENTINI received FDA 510(k) clearance on 1993-03-18, under 510(k) number K923884.

Who is the listed applicant for AUGUSTA VALENTINI?

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

What is the FDA product code for AUGUSTA VALENTINI?

The FDA product code for AUGUSTA VALENTINI is HQZ.

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Related Devices (Code: HQZ)

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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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