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)

MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET

K-Number: K852194 · 1985-09-27

ApplicantSharp Electronics Corp.
Decision Date1985-09-27
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET is the device name listed in this FDA 510(k) record. The listed applicant is Sharp Electronics Corp.. It received FDA 510(k) clearance on 1985-09-27 under 510(k) number K852194. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET?

MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET is a medical device that received FDA 510(k) clearance on 1985-09-27. The listed applicant is Sharp Electronics Corp.. The 510(k) number is K852194.

When did MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET receive FDA 510(k) clearance?

MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET received FDA 510(k) clearance on 1985-09-27, under 510(k) number K852194.

Who is the listed applicant for MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET?

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

What is the FDA product code for MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET?

The FDA product code for MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET is LHD.

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 Sharp Electronics Corp. 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.

K880715(MB-650) BLOOD PRESSURE MONITORK875093NEW MODEL MB-550 BLOOD PRESSURE MONITORK863672MODEL (MB-700) BLOOD PRESSURE MONITORK861375MODEL MB-500 & MB-600 BLOOD PRESSURE MONITORSK862333(MT-27) THERMOMETER AND (M-10PC) PROBE COVERSK851664MODEL MB-309H, SHARP DIGITAL BLOOD PRESSURE MONITO

View all 10 devices →

Related Devices (Code: LHD)

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.

K200163Ava Fertility TrackerAva AGK122337OVUSENSEFertility Focus, Ltd.K102499DUOFERTILITYCambridge Temperature Concepts , Ltd.K050094LADY COMP USALady Comp USAK030961MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921Microlife Corp.K021978PETIT SOPHIANishitomo Co., 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.

↑