STIKSEP-T4 RIA KIT
K-Number: K780423 · 1978-03-30
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Device Summary
Frequently Asked Questions
What is the STIKSEP-T4 RIA KIT?
STIKSEP-T4 RIA KIT is a medical device that received FDA 510(k) clearance on 1978-03-30. The listed applicant is Nuclear Diagnostics, Inc.. The 510(k) number is K780423.
When did STIKSEP-T4 RIA KIT receive FDA 510(k) clearance?
STIKSEP-T4 RIA KIT received FDA 510(k) clearance on 1978-03-30, under 510(k) number K780423.
Who is the listed applicant for STIKSEP-T4 RIA KIT?
The FDA 510(k) record lists Nuclear Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STIKSEP-T4 RIA KIT?
The FDA product code for STIKSEP-T4 RIA KIT is CDX.
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 Nuclear Diagnostics, Inc. 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: CDX)
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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