HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC KIT
K-Number: K946070 · 1996-01-30
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Device Summary
Frequently Asked Questions
What is the HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC KIT?
HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC KIT is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K946070.
When did HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC KIT receive FDA 510(k) clearance?
HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC KIT received FDA 510(k) clearance on 1996-01-30, under 510(k) number K946070.
Who is the listed applicant for HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC 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 MICROGLOBULIN TURBINDIMETRIC KIT?
The FDA product code for HUMAN BETA-2 MICROGLOBULIN TURBINDIMETRIC 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.
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
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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