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FDA 510(k)

PROBEYE THERMAL VIDEO SYSTEMS

K-Number: K843549 · 1985-02-11

Decision Date1985-02-11
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PROBEYE THERMAL VIDEO SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Hughes Aircraft Co.. It received FDA 510(k) clearance on 1985-02-11 under 510(k) number K843549. 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 PROBEYE THERMAL VIDEO SYSTEMS?

PROBEYE THERMAL VIDEO SYSTEMS is a medical device that received FDA 510(k) clearance on 1985-02-11. The listed applicant is Hughes Aircraft Co.. The 510(k) number is K843549.

When did PROBEYE THERMAL VIDEO SYSTEMS receive FDA 510(k) clearance?

PROBEYE THERMAL VIDEO SYSTEMS received FDA 510(k) clearance on 1985-02-11, under 510(k) number K843549.

Who is the listed applicant for PROBEYE THERMAL VIDEO SYSTEMS?

The FDA 510(k) record lists Hughes Aircraft Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROBEYE THERMAL VIDEO SYSTEMS?

The FDA product code for PROBEYE THERMAL VIDEO SYSTEMS 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.

Other records listing Hughes Aircraft 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.

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.

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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