CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676
K-Number: K952423 · 1995-06-22
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Device Summary
Frequently Asked Questions
What is the CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676?
CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676 is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Rolence Enterprise Co. , Ltd.. The 510(k) number is K952423.
When did CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676 receive FDA 510(k) clearance?
CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676 received FDA 510(k) clearance on 1995-06-22, under 510(k) number K952423.
Who is the listed applicant for CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676?
The FDA 510(k) record lists Rolence Enterprise Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676?
The FDA product code for CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676 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 Rolence Enterprise 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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