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FDA 510(k)

MEDHOT MTI 2000 THERMAL IMAGING SYSTEM

K-Number: K063047 · 2006-10-19

ApplicantMedhot Thermal Imaging, Inc.
Decision Date2006-10-19
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDHOT MTI 2000 THERMAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medhot Thermal Imaging, Inc.. It received FDA 510(k) clearance on 2006-10-19 under 510(k) number K063047. 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 MEDHOT MTI 2000 THERMAL IMAGING SYSTEM?

MEDHOT MTI 2000 THERMAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-19. The listed applicant is Medhot Thermal Imaging, Inc.. The 510(k) number is K063047.

When did MEDHOT MTI 2000 THERMAL IMAGING SYSTEM receive FDA 510(k) clearance?

MEDHOT MTI 2000 THERMAL IMAGING SYSTEM received FDA 510(k) clearance on 2006-10-19, under 510(k) number K063047.

Who is the listed applicant for MEDHOT MTI 2000 THERMAL IMAGING SYSTEM?

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

What is the FDA product code for MEDHOT MTI 2000 THERMAL IMAGING SYSTEM?

The FDA product code for MEDHOT MTI 2000 THERMAL IMAGING SYSTEM is LHQ.

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Related Devices (Code: 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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