ANALYTE T3 UPTAKE
K-Number: K802246 · 1980-10-23
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Device Summary
Frequently Asked Questions
What is the ANALYTE T3 UPTAKE?
ANALYTE T3 UPTAKE is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K802246.
When did ANALYTE T3 UPTAKE receive FDA 510(k) clearance?
ANALYTE T3 UPTAKE received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802246.
Who is the listed applicant for ANALYTE T3 UPTAKE?
The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANALYTE T3 UPTAKE?
The FDA product code for ANALYTE T3 UPTAKE is KHQ.
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 Technicon Instruments Corp. 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: KHQ)
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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