VECTORVISION
K-Number: K962939 · 1997-05-22
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Device Summary
Frequently Asked Questions
What is the VECTORVISION?
VECTORVISION is a medical device that received FDA 510(k) clearance on 1997-05-22. The listed applicant is Brainlab, Inc.. The 510(k) number is K962939.
When did VECTORVISION receive FDA 510(k) clearance?
VECTORVISION received FDA 510(k) clearance on 1997-05-22, under 510(k) number K962939.
Who is the listed applicant for VECTORVISION?
The FDA 510(k) record lists Brainlab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VECTORVISION?
The FDA product code for VECTORVISION is HAW.
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 Brainlab, 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: HAW)
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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