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)

MERCURY AND GLASS FEVER THERMOMETER

K-Number: K911269 · 1991-05-15

ApplicantSteridyne Corp.
Decision Date1991-05-15
Product CodeFLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MERCURY AND GLASS FEVER THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Steridyne Corp.. It received FDA 510(k) clearance on 1991-05-15 under 510(k) number K911269. 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 MERCURY AND GLASS FEVER THERMOMETER?

MERCURY AND GLASS FEVER THERMOMETER is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Steridyne Corp.. The 510(k) number is K911269.

When did MERCURY AND GLASS FEVER THERMOMETER receive FDA 510(k) clearance?

MERCURY AND GLASS FEVER THERMOMETER received FDA 510(k) clearance on 1991-05-15, under 510(k) number K911269.

Who is the listed applicant for MERCURY AND GLASS FEVER THERMOMETER?

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

What is the FDA product code for MERCURY AND GLASS FEVER THERMOMETER?

The FDA product code for MERCURY AND GLASS FEVER THERMOMETER 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

Other records listing Steridyne 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.

K925352CLEAN CUFF BLOOD PRESSURE CUFF LINERK911843ZERO-G(TM) GEL/FOAM MATTRESS TOPPERK842120ZERO-GK821314FEVER METERK801458WINTER HEAD DRESSING

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.

↑