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)

BAKER DIAG. ULTRARATE CHLORIDE KIT

K-Number: K802080 · 1980-10-10

ApplicantJ.T. Baker Chemical Co.
Decision Date1980-10-10
Product CodeJFS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BAKER DIAG. ULTRARATE CHLORIDE KIT is the device name listed in this FDA 510(k) record. The listed applicant is J.T. Baker Chemical Co.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802080. The device is classified under product code JFS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAKER DIAG. ULTRARATE CHLORIDE KIT?

BAKER DIAG. ULTRARATE CHLORIDE KIT is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K802080.

When did BAKER DIAG. ULTRARATE CHLORIDE KIT receive FDA 510(k) clearance?

BAKER DIAG. ULTRARATE CHLORIDE KIT received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802080.

Who is the listed applicant for BAKER DIAG. ULTRARATE CHLORIDE KIT?

The FDA 510(k) record lists J.T. Baker Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAKER DIAG. ULTRARATE CHLORIDE KIT?

The FDA product code for BAKER DIAG. ULTRARATE CHLORIDE KIT is JFS.

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 J.T. Baker Chemical Co. 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.

K803128SERIES 810 PLATELET ANALYZERK802035BAKER DIAG. ULTRARATE CO2 REAGENT KITK801909LSA 290 ASSAY REAGENTS/NEPHELOMETRICK801662J.T. BAKER ALPHA-2-MACROGLOBULIN NEPH.K801661J.T. BAKER CERULOPLASMIN NEPHELOMETRICK801795BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT.

View all 54 devices →

Related Devices (Code: JFS)

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.

K121823CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRICWescor, Inc.K923598REDI-CHECK PHOTMETER Q.A.Awareness Technology, Inc.K873127CHLORIDE REAGENT KITA-Kem, Inc.K830217REAGENTS CORNING CHLORIDE METER FORFisher Scientific Co., LLCK823106RERMCO TEST CHLORIDE REAGENTFermco Biochemics, Inc.K820411LIQUIZYME CHLORIDE REAGENTAmerican Research Products Co.

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.

↑