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FDA 510(k)

FLOW-PAC ALBUMIN REAGENT

K-Number: K830536 · 1983-03-24

ApplicantAmresco, Inc.
Decision Date1983-03-24
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLOW-PAC ALBUMIN REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Amresco, Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830536. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 39 devices →

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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