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)

YSI MODEL 2372 TOTAL BLOOD LACTATE KIT

K-Number: K852261 · 1985-08-15

ApplicantYellow Springs Instrument Co., Inc.
Decision Date1985-08-15
Product CodeKHP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

YSI MODEL 2372 TOTAL BLOOD LACTATE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Yellow Springs Instrument Co., Inc.. It received FDA 510(k) clearance on 1985-08-15 under 510(k) number K852261. The device is classified under product code KHP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI MODEL 2372 TOTAL BLOOD LACTATE KIT?

YSI MODEL 2372 TOTAL BLOOD LACTATE KIT is a medical device that received FDA 510(k) clearance on 1985-08-15. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K852261.

When did YSI MODEL 2372 TOTAL BLOOD LACTATE KIT receive FDA 510(k) clearance?

YSI MODEL 2372 TOTAL BLOOD LACTATE KIT received FDA 510(k) clearance on 1985-08-15, under 510(k) number K852261.

Who is the listed applicant for YSI MODEL 2372 TOTAL BLOOD LACTATE KIT?

The FDA 510(k) record lists Yellow Springs Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YSI MODEL 2372 TOTAL BLOOD LACTATE KIT?

The FDA product code for YSI MODEL 2372 TOTAL BLOOD LACTATE KIT is KHP.

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 Yellow Springs Instrument Co., Inc. 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.

K962070YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBEK922821YSI MODELS 4700 FOLEY CATHETER TEMPERATURE PROBESK922007YSI MODEL 441A AIRWAY TEMPERATURE PROBEK910633YSI MODEL 1500 BLOOD GLUCOSE ANALYZERK910718YSI PRECISION 4000 THERMOMETERK901131YSI MODEL 1500 SPORT L-LACTATE ANALYZER

View all 23 devices →

Related Devices (Code: KHP)

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.

K130113PICCOLO LACTATE TEST SYSTEMAbaxis, Inc.K113216RAPIDPOINT 500 BLOOD GAS ANALYERSiemens Healthcare DiagnosticsK112955NOVA STATSTRIP LACTATE HOSPITAL METER SYSTEMNova Biomedical CorporationK112430I-STAT LACTATE TEST/I-SAT CG4+CARTRIDGEAbbott Pont of Care, Inc.K100602NOVA STATSTRIP LACTATE HOSPITAL METER, NOVA STATSTRIP LACTATE TEST STRIPSNova Biomedical Corp.K093297EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBEEpocal, 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.

↑