FLOW-PAC ALBUMIN REAGENT
K-Number: K830536 · 1983-03-24
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Device Summary
Frequently Asked Questions
What is the FLOW-PAC ALBUMIN REAGENT?
FLOW-PAC ALBUMIN REAGENT is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Amresco, Inc.. The 510(k) number is K830536.
When did FLOW-PAC ALBUMIN REAGENT receive FDA 510(k) clearance?
FLOW-PAC ALBUMIN REAGENT received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830536.
Who is the listed applicant for FLOW-PAC ALBUMIN REAGENT?
The FDA 510(k) record lists Amresco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOW-PAC ALBUMIN REAGENT?
The FDA product code for FLOW-PAC ALBUMIN REAGENT is CIX.
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 Amresco, Inc. 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: CIX)
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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