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FDA 510(k)

RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN

K-Number: K792314 · 1979-12-06

Decision Date1979-12-06
Product CodeFAM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792314. The device is classified under product code FAM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN?

RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Icl Scientific. The 510(k) number is K792314.

When did RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN receive FDA 510(k) clearance?

RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792314.

Who is the listed applicant for RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN?

The FDA 510(k) record lists Icl Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN?

The FDA product code for RID SYSTEMS - ALPH-1-ACID GLYCOPROTEIN is FAM.

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 Icl Scientific 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 48 devices →

Related Devices (Code: FAM)

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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