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)

THERMOMETER, MERCURY/CLINICAL

K-Number: K883573 · 1988-11-07

ApplicantUmax Corp.
Decision Date1988-11-07
Product CodeFLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THERMOMETER, MERCURY/CLINICAL is the device name listed in this FDA 510(k) record. The listed applicant is Umax Corp.. It received FDA 510(k) clearance on 1988-11-07 under 510(k) number K883573. The device is classified under product code FLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOMETER, MERCURY/CLINICAL?

THERMOMETER, MERCURY/CLINICAL is a medical device that received FDA 510(k) clearance on 1988-11-07. The listed applicant is Umax Corp.. The 510(k) number is K883573.

When did THERMOMETER, MERCURY/CLINICAL receive FDA 510(k) clearance?

THERMOMETER, MERCURY/CLINICAL received FDA 510(k) clearance on 1988-11-07, under 510(k) number K883573.

Who is the listed applicant for THERMOMETER, MERCURY/CLINICAL?

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

What is the FDA product code for THERMOMETER, MERCURY/CLINICAL?

The FDA product code for THERMOMETER, MERCURY/CLINICAL is FLK.

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: FLK)

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.

K960185AMSINO CLINICAL THERMOMETERAmsia Intl., Inc.K960224GERATHERM MERCUIRY FREE CLINICAL THERMOMETERRg Ent., Inc.K953465KENTEMPKentron Health Care, Inc.K942483CLINICAL GLASS THERMOMETERMakol Medical Instruments Corp.K941673MEDIAID UNIVERSAL THERMOMETERPolymedica Industries, Inc.K940394AMG MED BRAND CLINICAL GLASS THERMOMETERTechnolab Industries (Canada) , 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.

↑