Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FEVER LINE AND FEVER LINE PLUS

K-Number: K893803 · 1989-08-21

ApplicantLiquid Crystal Sciences, Inc.
Decision Date1989-08-21
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FEVER LINE AND FEVER LINE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Liquid Crystal Sciences, Inc.. It received FDA 510(k) clearance on 1989-08-21 under 510(k) number K893803. 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 FEVER LINE AND FEVER LINE PLUS?

FEVER LINE AND FEVER LINE PLUS is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Liquid Crystal Sciences, Inc.. The 510(k) number is K893803.

When did FEVER LINE AND FEVER LINE PLUS receive FDA 510(k) clearance?

FEVER LINE AND FEVER LINE PLUS received FDA 510(k) clearance on 1989-08-21, under 510(k) number K893803.

Who is the listed applicant for FEVER LINE AND FEVER LINE PLUS?

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

What is the FDA product code for FEVER LINE AND FEVER LINE PLUS?

The FDA product code for FEVER LINE AND FEVER LINE PLUS is KPD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.K864853OMNI THERM TEMPERATURE MONITOROmni Therm, Inc.K850797TEMPALERT LIQUID CRYSTAL THERMOMETERMedical Frontiers, Inc.K841913TEMPTREND PEDS AXILLARY TEMP. INDICATORBiosynergy, Inc.K833904TEMPTREND IIBiosynergy, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑