T-3 UPTAKE (MAA) KIT
K-Number: K790461 · 1979-05-03
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Device Summary
Frequently Asked Questions
What is the T-3 UPTAKE (MAA) KIT?
T-3 UPTAKE (MAA) KIT is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Amersham Corp.. The 510(k) number is K790461.
When did T-3 UPTAKE (MAA) KIT receive FDA 510(k) clearance?
T-3 UPTAKE (MAA) KIT received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790461.
Who is the listed applicant for T-3 UPTAKE (MAA) KIT?
The FDA 510(k) record lists Amersham Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T-3 UPTAKE (MAA) KIT?
The FDA product code for T-3 UPTAKE (MAA) KIT 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 Amersham 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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