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FDA 510(k)

KIMAX QMA

K-Number: K022585 · 2002-10-11

ApplicantMedical Metrics, Inc.
Decision Date2002-10-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KIMAX QMA is the device name listed in this FDA 510(k) record. The listed applicant is Medical Metrics, Inc.. It received FDA 510(k) clearance on 2002-10-11 under 510(k) number K022585. 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 KIMAX QMA?

KIMAX QMA is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K022585.

When did KIMAX QMA receive FDA 510(k) clearance?

KIMAX QMA received FDA 510(k) clearance on 2002-10-11, under 510(k) number K022585.

Who is the listed applicant for KIMAX QMA?

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

What is the FDA product code for KIMAX QMA?

The FDA product code for KIMAX QMA is LLZ.

Related Clinical Trials

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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Other records listing Medical Metrics, 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.

K231668Spine CAMP™ (1.1)K221632Spine CAMP™K013098KIMAX REMOTE VIEWING STATIONK010187KIMAX, MODEL 1024

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

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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