VIDA LED SURGICAL LIGHTING SYSTEM
K-Number: K132307 · 2013-11-05
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Device Summary
Frequently Asked Questions
What is the VIDA LED SURGICAL LIGHTING SYSTEM?
VIDA LED SURGICAL LIGHTING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-11-05. The listed applicant is Convida Healthcare & Systems Corporation. The 510(k) number is K132307.
When did VIDA LED SURGICAL LIGHTING SYSTEM receive FDA 510(k) clearance?
VIDA LED SURGICAL LIGHTING SYSTEM received FDA 510(k) clearance on 2013-11-05, under 510(k) number K132307.
Who is the listed applicant for VIDA LED SURGICAL LIGHTING SYSTEM?
The FDA 510(k) record lists Convida Healthcare & Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIDA LED SURGICAL LIGHTING SYSTEM?
The FDA product code for VIDA LED SURGICAL LIGHTING SYSTEM is FSY.
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.
Related Devices (Code: FSY)
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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