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FDA 510(k)

J&S PEDIATRIC IRON SATURATING REAGENT

K-Number: K910672 · 1991-04-29

Decision Date1991-04-29
Product CodeJQE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

J&S PEDIATRIC IRON SATURATING REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is J.S. Medical Assoc.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K910672. The device is classified under product code JQE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J&S PEDIATRIC IRON SATURATING REAGENT?

J&S PEDIATRIC IRON SATURATING REAGENT is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K910672.

When did J&S PEDIATRIC IRON SATURATING REAGENT receive FDA 510(k) clearance?

J&S PEDIATRIC IRON SATURATING REAGENT received FDA 510(k) clearance on 1991-04-29, under 510(k) number K910672.

Who is the listed applicant for J&S PEDIATRIC IRON SATURATING REAGENT?

The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for J&S PEDIATRIC IRON SATURATING REAGENT?

The FDA product code for J&S PEDIATRIC IRON SATURATING REAGENT is JQE.

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 J.S. Medical Assoc. 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.

View all 18 devices →

Related Devices (Code: JQE)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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