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)

MULTICHANNEL 2000 FLUOROPTIC THERMOMET

K-Number: K841105 · 1984-07-03

ApplicantLuxtron
Decision Date1984-07-03
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTICHANNEL 2000 FLUOROPTIC THERMOMET is the device name listed in this FDA 510(k) record. The listed applicant is Luxtron. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K841105. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICHANNEL 2000 FLUOROPTIC THERMOMET?

MULTICHANNEL 2000 FLUOROPTIC THERMOMET is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Luxtron. The 510(k) number is K841105.

When did MULTICHANNEL 2000 FLUOROPTIC THERMOMET receive FDA 510(k) clearance?

MULTICHANNEL 2000 FLUOROPTIC THERMOMET received FDA 510(k) clearance on 1984-07-03, under 510(k) number K841105.

Who is the listed applicant for MULTICHANNEL 2000 FLUOROPTIC THERMOMET?

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

What is the FDA product code for MULTICHANNEL 2000 FLUOROPTIC THERMOMET?

The FDA product code for MULTICHANNEL 2000 FLUOROPTIC THERMOMET is FLL.

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

Other records listing Luxtron 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.

K923189LUXTRON MODEL 3100/3101/3102 MULTICHANNELK861623MODEL 3000 MLULTICHANNEL FLUOROPTIC THERMOMETERK821070BIOMEDICAL FLUOROPTIC

Related Devices (Code: FLL)

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.

K253162Temperature probes (T2252-PG); Temperature probes (TCMA-AG); Temperature probes (TCMA-PG); Temperature probes (TMQ-DAG); Temperature probes (THP-DAG)Unimed Medical Supplies, Inc.K251160Sterile temperature probe (Model: W0001ES, W0028ES, W0101FS-A, W0101FS-P, W0099LS, W0099FS, W0099PS)Shenzhen Med-Link Electronics Tech Co., Ltd.K250470Ear Thermometer (EAR-E101); Ear Thermometer (EAR-E102); Ear Thermometer (EAR-E103)Shenzhen AOJ Medical Technology Co., Ltd.K243000Reusable Temperature Probe (T1306, T2306, T3306, T4306); Disposable Temperature Probe (T5106, T6106)Shenzhen Medke Technology Co., Ltd.K250878YUWELL® Infrared Ear Thermometer (YHT100); YUWELL® Infrared Ear Thermometer (YHT107)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.K243082Infrared ThermometerGuangzhou Daxin Health Technology Co., Ltd.

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.

↑