VISUM LED SURGICAL LIGHTING SYSTEM
K-Number: K060802 · 2006-04-07
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Device Summary
Frequently Asked Questions
What is the VISUM LED SURGICAL LIGHTING SYSTEM?
VISUM LED SURGICAL LIGHTING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-04-07. The listed applicant is Stryker Communications Corp.. The 510(k) number is K060802.
When did VISUM LED SURGICAL LIGHTING SYSTEM receive FDA 510(k) clearance?
VISUM LED SURGICAL LIGHTING SYSTEM received FDA 510(k) clearance on 2006-04-07, under 510(k) number K060802.
Who is the listed applicant for VISUM LED SURGICAL LIGHTING SYSTEM?
The FDA 510(k) record lists Stryker Communications Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISUM LED SURGICAL LIGHTING SYSTEM?
The FDA product code for VISUM 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.
Other records listing Stryker Communications 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: 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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