J & S IRON SATURATING REAGENT
K-Number: K811942 · 1981-09-08
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Device Summary
Frequently Asked Questions
What is the J & S IRON SATURATING REAGENT?
J & S IRON SATURATING REAGENT is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Thyroid Diagnostics, Inc.. The 510(k) number is K811942.
When did J & S IRON SATURATING REAGENT receive FDA 510(k) clearance?
J & S IRON SATURATING REAGENT received FDA 510(k) clearance on 1981-09-08, under 510(k) number K811942.
Who is the listed applicant for J & S IRON SATURATING REAGENT?
The FDA 510(k) record lists Thyroid Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for J & S IRON SATURATING REAGENT?
The FDA product code for J & S IRON SATURATING REAGENT is JQF.
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 Thyroid 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: JQF)
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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