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FDA 510(k)

AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500

K-Number: K900977 · 1990-04-11

ApplicantAmerican Research Products Co.
Decision Date1990-04-11
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500 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 1990-04-11 under 510(k) number K900977. 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 AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500?

AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500 is a medical device that received FDA 510(k) clearance on 1990-04-11. The listed applicant is American Research Products Co.. The 510(k) number is K900977.

When did AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500 receive FDA 510(k) clearance?

AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500 received FDA 510(k) clearance on 1990-04-11, under 510(k) number K900977.

Who is the listed applicant for AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500?

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 AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500?

The FDA product code for AMRESCO INORGANIC PHOSPHORUS PRODUCT #4312500 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)

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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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