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FDA 510(k)

DIAG. CONDUCTA RATE BUN REAG. SET

K-Number: K771060 · 1977-07-21

ApplicantJ.T. Baker Chemical Co.
Decision Date1977-07-21
Product CodeCDS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIAG. CONDUCTA RATE BUN REAG. SET 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 1977-07-21 under 510(k) number K771060. The device is classified under product code CDS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAG. CONDUCTA RATE BUN REAG. SET?

DIAG. CONDUCTA RATE BUN REAG. SET is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K771060.

When did DIAG. CONDUCTA RATE BUN REAG. SET receive FDA 510(k) clearance?

DIAG. CONDUCTA RATE BUN REAG. SET received FDA 510(k) clearance on 1977-07-21, under 510(k) number K771060.

Who is the listed applicant for DIAG. CONDUCTA RATE BUN REAG. SET?

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 DIAG. CONDUCTA RATE BUN REAG. SET?

The FDA product code for DIAG. CONDUCTA RATE BUN REAG. SET is CDS.

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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 ANALYZERK802080BAKER DIAG. ULTRARATE CHLORIDE KITK801909LSA 290 ASSAY REAGENTS/NEPHELOMETRICK802035BAKER DIAG. ULTRARATE CO2 REAGENT KITK801795BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT.K801661J.T. BAKER CERULOPLASMIN NEPHELOMETRIC

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Related Devices (Code: CDS)

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.

K171247epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide TestEpocal, Inc.K040973BUN REAGENTGenchem, Inc.K033056BUN REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA REAGENTDiamond Diagnostics, Inc.K925550HI CHEM BUN REAGENT KIT,PRODUCT NUMBER 88806Hichem DiagnosticsK860543BLOOD UREA NITROGEN (BUN) TESTCARDIlex Corp.K855091CHEM-PRO 1000 CLINICAL CHEMISTRY-ANALYSIS SYSSen Tech Medical Corp.

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.

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