T-3 UPTAKE (SORBENT) KIT
K-Number: K780525 · 1978-05-19
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Device Summary
Frequently Asked Questions
What is the T-3 UPTAKE (SORBENT) KIT?
T-3 UPTAKE (SORBENT) KIT is a medical device that received FDA 510(k) clearance on 1978-05-19. The listed applicant is Amersham Corp.. The 510(k) number is K780525.
When did T-3 UPTAKE (SORBENT) KIT receive FDA 510(k) clearance?
T-3 UPTAKE (SORBENT) KIT received FDA 510(k) clearance on 1978-05-19, under 510(k) number K780525.
Who is the listed applicant for T-3 UPTAKE (SORBENT) 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 (SORBENT) KIT?
The FDA product code for T-3 UPTAKE (SORBENT) 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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