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FDA 510(k)

SUNRISE CURING LAMP

K-Number: K962192 · 1996-09-03

ApplicantSunrise Technologies, Inc.
Decision Date1996-09-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUNRISE CURING LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Technologies, Inc.. It received FDA 510(k) clearance on 1996-09-03 under 510(k) number K962192. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNRISE CURING LAMP?

SUNRISE CURING LAMP is a medical device that received FDA 510(k) clearance on 1996-09-03. The listed applicant is Sunrise Technologies, Inc.. The 510(k) number is K962192.

When did SUNRISE CURING LAMP receive FDA 510(k) clearance?

SUNRISE CURING LAMP received FDA 510(k) clearance on 1996-09-03, under 510(k) number K962192.

Who is the listed applicant for SUNRISE CURING LAMP?

The FDA 510(k) record lists Sunrise Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNRISE CURING LAMP?

The FDA product code for SUNRISE CURING LAMP is EBF.

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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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