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FDA 510(k)

DW 296 #15 SOLDER

K-Number: K032715 · 2003-09-26

ApplicantIvoclar Vivadent, Inc.
Decision Date2003-09-26
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DW 296 #15 SOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2003-09-26 under 510(k) number K032715. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW 296 #15 SOLDER?

DW 296 #15 SOLDER is a medical device that received FDA 510(k) clearance on 2003-09-26. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K032715.

When did DW 296 #15 SOLDER receive FDA 510(k) clearance?

DW 296 #15 SOLDER received FDA 510(k) clearance on 2003-09-26, under 510(k) number K032715.

Who is the listed applicant for DW 296 #15 SOLDER?

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

What is the FDA product code for DW 296 #15 SOLDER?

The FDA product code for DW 296 #15 SOLDER is EJT.

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Related Devices (Code: EJT)

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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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