RIASET PROLACTIN RIA KIT
K-Number: K823304 · 1982-12-22
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Device Summary
Frequently Asked Questions
What is the RIASET PROLACTIN RIA KIT?
RIASET PROLACTIN RIA KIT is a medical device that received FDA 510(k) clearance on 1982-12-22. The listed applicant is Immulok, Inc.. The 510(k) number is K823304.
When did RIASET PROLACTIN RIA KIT receive FDA 510(k) clearance?
RIASET PROLACTIN RIA KIT received FDA 510(k) clearance on 1982-12-22, under 510(k) number K823304.
Who is the listed applicant for RIASET PROLACTIN RIA KIT?
The FDA 510(k) record lists Immulok, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIASET PROLACTIN RIA KIT?
The FDA product code for RIASET PROLACTIN RIA KIT is CFT.
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 Immulok, 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: CFT)
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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