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FDA 510(k)

TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB

K-Number: K020783 · 2002-06-07

ApplicantTelesis Technologies, Inc.
Decision Date2002-06-07
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB is the device name listed in this FDA 510(k) record. The listed applicant is Telesis Technologies, Inc.. It received FDA 510(k) clearance on 2002-06-07 under 510(k) number K020783. The device is classified under product code LHQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB?

TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB is a medical device that received FDA 510(k) clearance on 2002-06-07. The listed applicant is Telesis Technologies, Inc.. The 510(k) number is K020783.

When did TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB receive FDA 510(k) clearance?

TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB received FDA 510(k) clearance on 2002-06-07, under 510(k) number K020783.

Who is the listed applicant for TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB?

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

What is the FDA product code for TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB?

The FDA product code for TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB is LHQ.

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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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