DIALOG WITH ADIMEA OPTION
K-Number: K083460 · 2010-02-18
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Device Summary
Frequently Asked Questions
What is the DIALOG WITH ADIMEA OPTION?
DIALOG WITH ADIMEA OPTION is a medical device that received FDA 510(k) clearance on 2010-02-18. The listed applicant is B. Braun Avitum AG. The 510(k) number is K083460.
When did DIALOG WITH ADIMEA OPTION receive FDA 510(k) clearance?
DIALOG WITH ADIMEA OPTION received FDA 510(k) clearance on 2010-02-18, under 510(k) number K083460.
Who is the listed applicant for DIALOG WITH ADIMEA OPTION?
The FDA 510(k) record lists B. Braun Avitum AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIALOG WITH ADIMEA OPTION?
The FDA product code for DIALOG WITH ADIMEA OPTION is KDI.
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 B. Braun Avitum AG 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: KDI)
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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