CONTEC LIGHT
K-Number: K030641 · 2003-06-10
Advertisement
Device Summary
Frequently Asked Questions
What is the CONTEC LIGHT?
CONTEC LIGHT is a medical device that received FDA 510(k) clearance on 2003-06-10. The listed applicant is Dentaurum. The 510(k) number is K030641.
When did CONTEC LIGHT receive FDA 510(k) clearance?
CONTEC LIGHT received FDA 510(k) clearance on 2003-06-10, under 510(k) number K030641.
Who is the listed applicant for CONTEC LIGHT?
The FDA 510(k) record lists Dentaurum as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTEC LIGHT?
The FDA product code for CONTEC 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 Dentaurum 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.
Advertisement