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FDA 510(k)

AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781

K-Number: K900250 · 1990-03-01

Decision Date1990-03-01
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781 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 1990-03-01 under 510(k) number K900250. The device is classified under product code CJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781?

AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781 is a medical device that received FDA 510(k) clearance on 1990-03-01. The listed applicant is American Research Products Co.. The 510(k) number is K900250.

When did AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781 receive FDA 510(k) clearance?

AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781 received FDA 510(k) clearance on 1990-03-01, under 510(k) number K900250.

Who is the listed applicant for AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781?

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 ALKALINE PHOSPHATASE REAGENTS 7780 & 7781?

The FDA product code for AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781 is CJE.

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.

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.

View all 56 devices →

Related Devices (Code: CJE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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