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FDA 510(k)

OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM

K-Number: K925961 · 1993-03-02

ApplicantDiagnostic Archives, Inc.
Decision Date1993-03-02
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Archives, Inc.. It received FDA 510(k) clearance on 1993-03-02 under 510(k) number K925961. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM?

OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-02. The listed applicant is Diagnostic Archives, Inc.. The 510(k) number is K925961.

When did OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM receive FDA 510(k) clearance?

OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM received FDA 510(k) clearance on 1993-03-02, under 510(k) number K925961.

Who is the listed applicant for OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM?

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

What is the FDA product code for OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM?

The FDA product code for OPTIMA ARCHIVAL AND RETRIEVAL SYSTEM is IZI.

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Related Devices (Code: IZI)

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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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