ENCORE PROLACTIN REAGENT
K-Number: K860221 · 1986-03-05
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Device Summary
Frequently Asked Questions
What is the ENCORE PROLACTIN REAGENT?
ENCORE PROLACTIN REAGENT is a medical device that received FDA 510(k) clearance on 1986-03-05. The listed applicant is Hybritech, Inc.. The 510(k) number is K860221.
When did ENCORE PROLACTIN REAGENT receive FDA 510(k) clearance?
ENCORE PROLACTIN REAGENT received FDA 510(k) clearance on 1986-03-05, under 510(k) number K860221.
Who is the listed applicant for ENCORE PROLACTIN REAGENT?
The FDA 510(k) record lists Hybritech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENCORE PROLACTIN REAGENT?
The FDA product code for ENCORE PROLACTIN REAGENT 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 Hybritech, 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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