J&S UIBC REAGENTS
K-Number: K912717 · 1991-09-25
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Device Summary
Frequently Asked Questions
What is the J&S UIBC REAGENTS?
J&S UIBC REAGENTS is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K912717.
When did J&S UIBC REAGENTS receive FDA 510(k) clearance?
J&S UIBC REAGENTS received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912717.
Who is the listed applicant for J&S UIBC REAGENTS?
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 UIBC REAGENTS?
The FDA product code for J&S UIBC REAGENTS 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 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.
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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