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FDA 510(k)

KIMAX REMOTE VIEWING STATION

K-Number: K013098 · 2001-12-07

Decision Date2001-12-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KIMAX REMOTE VIEWING STATION 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 2001-12-07 under 510(k) number K013098. 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 REMOTE VIEWING STATION?

KIMAX REMOTE VIEWING STATION is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K013098.

When did KIMAX REMOTE VIEWING STATION receive FDA 510(k) clearance?

KIMAX REMOTE VIEWING STATION received FDA 510(k) clearance on 2001-12-07, under 510(k) number K013098.

Who is the listed applicant for KIMAX REMOTE VIEWING STATION?

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 REMOTE VIEWING STATION?

The FDA product code for KIMAX REMOTE VIEWING STATION 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.

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.

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.

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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