DIB INFUSOR
K-Number: K930404 · 1994-02-25
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Device Summary
Frequently Asked Questions
What is the DIB INFUSOR?
DIB INFUSOR is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Novacon Corp.. The 510(k) number is K930404.
When did DIB INFUSOR receive FDA 510(k) clearance?
DIB INFUSOR received FDA 510(k) clearance on 1994-02-25, under 510(k) number K930404.
Who is the listed applicant for DIB INFUSOR?
The FDA 510(k) record lists Novacon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIB INFUSOR?
The FDA product code for DIB INFUSOR is MEB.
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 Novacon Corp. 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: MEB)
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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