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FDA 510(k)

LIQUID CRYSTAL THERMOGRAPHIC SYSTEM

K-Number: K780478 · 1978-10-02

Decision Date1978-10-02
Product Code
DecisionSubstantially Equivalent

Device Summary

LIQUID CRYSTAL THERMOGRAPHIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Thermal Imagery, Inc.. It received FDA 510(k) clearance on 1978-10-02 under 510(k) number K780478. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CRYSTAL THERMOGRAPHIC SYSTEM?

LIQUID CRYSTAL THERMOGRAPHIC SYSTEM is a medical device that received FDA 510(k) clearance on 1978-10-02. The listed applicant is Thermal Imagery, Inc.. The 510(k) number is K780478.

When did LIQUID CRYSTAL THERMOGRAPHIC SYSTEM receive FDA 510(k) clearance?

LIQUID CRYSTAL THERMOGRAPHIC SYSTEM received FDA 510(k) clearance on 1978-10-02, under 510(k) number K780478.

Who is the listed applicant for LIQUID CRYSTAL THERMOGRAPHIC SYSTEM?

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

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.

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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