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FDA 510(k)

MRI PROLACTIN RIA KIT

K-Number: K810949 · 1981-07-10

Decision Date1981-07-10
Product CodeCFT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MRI PROLACTIN RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Microanalytic Research, Inc.. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K810949. The device is classified under product code CFT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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