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FDA 510(k)

COLORIMETRIC CHLORIDE PRODUCT #4314125

K-Number: K900827 · 1990-05-02

ApplicantAmerican Research Products Co.
Decision Date1990-05-02
Product CodeCHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COLORIMETRIC CHLORIDE PRODUCT #4314125 is the device name listed in this FDA 510(k) record. The listed applicant is American Research Products Co.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K900827. The device is classified under product code CHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLORIMETRIC CHLORIDE PRODUCT #4314125?

COLORIMETRIC CHLORIDE PRODUCT #4314125 is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is American Research Products Co.. The 510(k) number is K900827.

When did COLORIMETRIC CHLORIDE PRODUCT #4314125 receive FDA 510(k) clearance?

COLORIMETRIC CHLORIDE PRODUCT #4314125 received FDA 510(k) clearance on 1990-05-02, under 510(k) number K900827.

Who is the listed applicant for COLORIMETRIC CHLORIDE PRODUCT #4314125?

The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLORIMETRIC CHLORIDE PRODUCT #4314125?

The FDA product code for COLORIMETRIC CHLORIDE PRODUCT #4314125 is CHI.

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Other records listing American Research Products 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.

K942984BUN REAGENTK901527BIURET (COLORMETRIC), TOTAL PROTEINK901960IRON REAGENTS PRODUCT CODES 7725 AND 7726K901964PHOSPHORUS REAGENTS PROD CODES 7763/7764/7563/7463K901702NAD REDUCTION, ALT/SPGT CODES 7722,7723,7422,7522K900666AMRESCO CREATININE REAGENTS PRODUCT #7790, 7791

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Related Devices (Code: CHI)

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.

K970905SYNCHRON CX SYSTEMS LIPASE (LIPA) REAGENTBeckman Instruments, Inc.K961179SENTINEL LIPASE LIQUID MODEL 17.401BEqual Diagnostics, Inc.K952180CX LIPASE REAGENT & CALIBRATOR FOR SYNCHRON CX SYSTEMSBeckman Instruments, Inc.K952647IL TEST LIPASEInstrumentation Laboratory COK952816LIPASE FLEX REAGENT CARTRIDGEDupont Medical ProductsK941085LIPASE-PS ASSAY PROCEDURE NO. 805Sigma Diagnostics, 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.

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