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FDA 510(k)

DMI CONSOLE

K-Number: K844317 · 1985-02-26

ApplicantDimensional Medicine, Inc.
Decision Date1985-02-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DMI CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is Dimensional Medicine, Inc.. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K844317. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMI CONSOLE?

DMI CONSOLE is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Dimensional Medicine, Inc.. The 510(k) number is K844317.

When did DMI CONSOLE receive FDA 510(k) clearance?

DMI CONSOLE received FDA 510(k) clearance on 1985-02-26, under 510(k) number K844317.

Who is the listed applicant for DMI CONSOLE?

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

What is the FDA product code for DMI CONSOLE?

The FDA product code for DMI CONSOLE is LLZ.

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Other records listing Dimensional Medicine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932564RADSTATK930500MAXIVIEW DIAGNOSTIC WORKSTATIONK920851MACVIEW

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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