IMMPULSE FERRITIN ASSAY REAGENT
K-Number: K862014 · 1986-06-19
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Device Summary
Frequently Asked Questions
What is the IMMPULSE FERRITIN ASSAY REAGENT?
IMMPULSE FERRITIN ASSAY REAGENT is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Sclavo, Inc.. The 510(k) number is K862014.
When did IMMPULSE FERRITIN ASSAY REAGENT receive FDA 510(k) clearance?
IMMPULSE FERRITIN ASSAY REAGENT received FDA 510(k) clearance on 1986-06-19, under 510(k) number K862014.
Who is the listed applicant for IMMPULSE FERRITIN ASSAY REAGENT?
The FDA 510(k) record lists Sclavo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMMPULSE FERRITIN ASSAY REAGENT?
The FDA product code for IMMPULSE FERRITIN ASSAY REAGENT is DBF.
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 Sclavo, 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: DBF)
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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