Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676

K-Number: K952423 · 1995-06-22

Decision Date1995-06-22
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676 is the device name listed in this FDA 510(k) record. The listed applicant is Rolence Enterprise Co. , Ltd.. It received FDA 510(k) clearance on 1995-06-22 under 510(k) number K952423. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 12 devices →

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.

↑