DIB INFUSORS
K-Number: K944665 · 1995-02-14
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Device Summary
Frequently Asked Questions
What is the DIB INFUSORS?
DIB INFUSORS is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Novacon Corp.. The 510(k) number is K944665.
When did DIB INFUSORS receive FDA 510(k) clearance?
DIB INFUSORS received FDA 510(k) clearance on 1995-02-14, under 510(k) number K944665.
Who is the listed applicant for DIB INFUSORS?
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 INFUSORS?
The FDA product code for DIB INFUSORS 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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