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FDA 510(k)

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM

K-Number: K032471 · 2003-10-10

ApplicantTitronics Research & Development Co.
Decision Date2003-10-10
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Titronics Research & Development Co.. It received FDA 510(k) clearance on 2003-10-10 under 510(k) number K032471. 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 TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM?

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-10. The listed applicant is Titronics Research & Development Co.. The 510(k) number is K032471.

When did TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM receive FDA 510(k) clearance?

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM received FDA 510(k) clearance on 2003-10-10, under 510(k) number K032471.

Who is the listed applicant for TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM?

The FDA 510(k) record lists Titronics Research & Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM?

The FDA product code for TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM is LHQ.

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 Titronics Research & Development Co. 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.

K974208TYTRON C-3000

Related Devices (Code: LHQ)

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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