MSI-NAK-50 TEST KIT
K-Number: K831300 · 1983-07-18
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Device Summary
Frequently Asked Questions
What is the MSI-NAK-50 TEST KIT?
MSI-NAK-50 TEST KIT is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K831300.
When did MSI-NAK-50 TEST KIT receive FDA 510(k) clearance?
MSI-NAK-50 TEST KIT received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831300.
Who is the listed applicant for MSI-NAK-50 TEST KIT?
The FDA 510(k) record lists Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MSI-NAK-50 TEST KIT?
The FDA product code for MSI-NAK-50 TEST KIT is JGM.
Other records listing Medical Specialties, 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: JGM)
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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