BRACHYVISION 6.0
K-Number: K992762 · 2000-03-09
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Device Summary
Frequently Asked Questions
What is the BRACHYVISION 6.0?
BRACHYVISION 6.0 is a medical device that received FDA 510(k) clearance on 2000-03-09. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K992762.
When did BRACHYVISION 6.0 receive FDA 510(k) clearance?
BRACHYVISION 6.0 received FDA 510(k) clearance on 2000-03-09, under 510(k) number K992762.
Who is the listed applicant for BRACHYVISION 6.0?
The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRACHYVISION 6.0?
The FDA product code for BRACHYVISION 6.0 is MUJ.
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 Varian Assoc., 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: MUJ)
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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