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FDA 510(k)

HUMAN BETA-2 MICROGLOBIN EN-RID KIT

K-Number: K913131 · 1991-11-07

Decision Date1991-11-07
Product CodeJZG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

HUMAN BETA-2 MICROGLOBIN EN-RID KIT is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site, Ltd.. It received FDA 510(k) clearance on 1991-11-07 under 510(k) number K913131. The device is classified under product code JZG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN BETA-2 MICROGLOBIN EN-RID KIT?

HUMAN BETA-2 MICROGLOBIN EN-RID KIT is a medical device that received FDA 510(k) clearance on 1991-11-07. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K913131.

When did HUMAN BETA-2 MICROGLOBIN EN-RID KIT receive FDA 510(k) clearance?

HUMAN BETA-2 MICROGLOBIN EN-RID KIT received FDA 510(k) clearance on 1991-11-07, under 510(k) number K913131.

Who is the listed applicant for HUMAN BETA-2 MICROGLOBIN EN-RID KIT?

The FDA 510(k) record lists The Binding Site, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMAN BETA-2 MICROGLOBIN EN-RID KIT?

The FDA product code for HUMAN BETA-2 MICROGLOBIN EN-RID KIT is JZG.

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 The Binding Site, Ltd. 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 115 devices →

Related Devices (Code: JZG)

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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