AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET
K-Number: K861968 · 1986-06-13
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Device Summary
Frequently Asked Questions
What is the AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET?
AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is American Research Products Co.. The 510(k) number is K861968.
When did AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET receive FDA 510(k) clearance?
AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET received FDA 510(k) clearance on 1986-06-13, under 510(k) number K861968.
Who is the listed applicant for AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET?
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 FLOW PAC INORGANIC PHOSPHRUS REAGENT SET?
The FDA product code for AMRESCO FLOW PAC INORGANIC PHOSPHRUS REAGENT SET is CEO.
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.
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.
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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