CYBIRD LED CURING LIGHT
K-Number: K042703 · 2004-10-12
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Device Summary
Frequently Asked Questions
What is the CYBIRD LED CURING LIGHT?
CYBIRD LED CURING LIGHT is a medical device that received FDA 510(k) clearance on 2004-10-12. The listed applicant is Dxm Co., Ltd.. The 510(k) number is K042703.
When did CYBIRD LED CURING LIGHT receive FDA 510(k) clearance?
CYBIRD LED CURING LIGHT received FDA 510(k) clearance on 2004-10-12, under 510(k) number K042703.
Who is the listed applicant for CYBIRD LED CURING LIGHT?
The FDA 510(k) record lists Dxm Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CYBIRD LED CURING LIGHT?
The FDA product code for CYBIRD LED CURING LIGHT is EBZ.
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 Dxm Co., Ltd. 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: EBZ)
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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