MRI PROLACTIN RIA KIT
K-Number: K810949 · 1981-07-10
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Device Summary
Frequently Asked Questions
What is the MRI PROLACTIN RIA KIT?
MRI PROLACTIN RIA KIT is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Microanalytic Research, Inc.. The 510(k) number is K810949.
When did MRI PROLACTIN RIA KIT receive FDA 510(k) clearance?
MRI PROLACTIN RIA KIT received FDA 510(k) clearance on 1981-07-10, under 510(k) number K810949.
Who is the listed applicant for MRI PROLACTIN RIA KIT?
The FDA 510(k) record lists Microanalytic Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRI PROLACTIN RIA KIT?
The FDA product code for MRI 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 Microanalytic Research, 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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