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FDA 510(k)

LIQUID CRYSTAL THERM. 8 EVENT MONITOR

K-Number: K802778 · 1981-01-09

ApplicantDjinnii Industires, Inc.
Decision Date1981-01-09
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIQUID CRYSTAL THERM. 8 EVENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Djinnii Industires, Inc.. It received FDA 510(k) clearance on 1981-01-09 under 510(k) number K802778. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CRYSTAL THERM. 8 EVENT MONITOR?

LIQUID CRYSTAL THERM. 8 EVENT MONITOR is a medical device that received FDA 510(k) clearance on 1981-01-09. The listed applicant is Djinnii Industires, Inc.. The 510(k) number is K802778.

When did LIQUID CRYSTAL THERM. 8 EVENT MONITOR receive FDA 510(k) clearance?

LIQUID CRYSTAL THERM. 8 EVENT MONITOR received FDA 510(k) clearance on 1981-01-09, under 510(k) number K802778.

Who is the listed applicant for LIQUID CRYSTAL THERM. 8 EVENT MONITOR?

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

What is the FDA product code for LIQUID CRYSTAL THERM. 8 EVENT MONITOR?

The FDA product code for LIQUID CRYSTAL THERM. 8 EVENT MONITOR is KPD.

Related Clinical Trials

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Related Devices (Code: KPD)

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.

K934941E-Z TEMP IISeven C'S, Inc.K903307TEMP MARQ TEMPERATURE TREND INDICATORMarquest Medical Products, Inc.K893803FEVER LINE AND FEVER LINE PLUSLiquid Crystal Sciences, Inc.K864853OMNI THERM TEMPERATURE MONITOROmni Therm, Inc.K850797TEMPALERT LIQUID CRYSTAL THERMOMETERMedical Frontiers, Inc.K841913TEMPTREND PEDS AXILLARY TEMP. INDICATORBiosynergy, Inc.

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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