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FDA 510(k)

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS

K-Number: K871321 · 1987-04-22

ApplicantAmerican Research Products Co.
Decision Date1987-04-22
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS 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 1987-04-22 under 510(k) number K871321. The device is classified under product code CEO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW-PAC INORGANIC PHOSPHORUS REAGENTS?

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS is a medical device that received FDA 510(k) clearance on 1987-04-22. The listed applicant is American Research Products Co.. The 510(k) number is K871321.

When did FLOW-PAC INORGANIC PHOSPHORUS REAGENTS receive FDA 510(k) clearance?

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS received FDA 510(k) clearance on 1987-04-22, under 510(k) number K871321.

Who is the listed applicant for FLOW-PAC INORGANIC PHOSPHORUS REAGENTS?

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 FLOW-PAC INORGANIC PHOSPHORUS REAGENTS?

The FDA product code for FLOW-PAC INORGANIC PHOSPHORUS REAGENTS is CEO.

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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 7763/7764/7563/7463K900827COLORIMETRIC CHLORIDE PRODUCT #4314125K901702NAD REDUCTION, ALT/SPGT CODES 7722,7723,7422,7522

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Related Devices (Code: CEO)

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.

K100263ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTSSeppim S.A.S.K072141S40 CLINICAL ANALYZER, S TEST IP, S TEST UAAlfa Wassermann Diagnostic Technologies, Inc.K041643SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENTBeckman Coulter, Inc.K030015ATAC PAK PHOSPHORUS REAGENTElan DiagnosticsK022312PICCOLO PHOSPHORUS TEST SYSTEMAbaxis, Inc.K013095WIENER LAB.FOSFATEMIA UV, MODELS 1X100 ML CAT.N 1382321, 4X20 ML CAT.N 1009311Wiener Laboratories Saic

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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