MSI PROCEDURE KIT
K-Number: K944226 · 1995-06-21
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Device Summary
Frequently Asked Questions
What is the MSI PROCEDURE KIT?
MSI PROCEDURE KIT is a medical device that received FDA 510(k) clearance on 1995-06-21. The listed applicant is Msi, Inc.. The 510(k) number is K944226.
When did MSI PROCEDURE KIT receive FDA 510(k) clearance?
MSI PROCEDURE KIT received FDA 510(k) clearance on 1995-06-21, under 510(k) number K944226.
Who is the listed applicant for MSI PROCEDURE KIT?
The FDA 510(k) record lists Msi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MSI PROCEDURE KIT?
The FDA product code for MSI PROCEDURE KIT is DOX.
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 Msi, 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: DOX)
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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