KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT
K-Number: K933329 · 1993-10-22
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Device Summary
Frequently Asked Questions
What is the KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT?
KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT is a medical device that received FDA 510(k) clearance on 1993-10-22. The listed applicant is King Diagnostics, Inc.. The 510(k) number is K933329.
When did KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT receive FDA 510(k) clearance?
KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT received FDA 510(k) clearance on 1993-10-22, under 510(k) number K933329.
Who is the listed applicant for KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT?
The FDA 510(k) record lists King Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT?
The FDA product code for KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT is JMO.
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 King Diagnostics, 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: JMO)
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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