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FDA 510(k)

SLED CURING LIGHT SYSTEM

K-Number: K031615 · 2003-07-21

ApplicantDentsply International
Decision Date2003-07-21
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SLED CURING LIGHT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K031615. 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 SLED CURING LIGHT SYSTEM?

SLED CURING LIGHT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is Dentsply International. The 510(k) number is K031615.

When did SLED CURING LIGHT SYSTEM receive FDA 510(k) clearance?

SLED CURING LIGHT SYSTEM received FDA 510(k) clearance on 2003-07-21, under 510(k) number K031615.

Who is the listed applicant for SLED CURING LIGHT SYSTEM?

The FDA 510(k) record lists Dentsply International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLED CURING LIGHT SYSTEM?

The FDA product code for SLED CURING LIGHT SYSTEM is EBZ.

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Other records listing Dentsply International as applicant

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Related Devices (Code: EBZ)

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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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