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FDA 510(k)

SR IVOCRON

K-Number: K013869 · 2002-08-28

ApplicantIvoclar Vivadent, Inc.
Decision Date2002-08-28
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SR IVOCRON 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 2002-08-28 under 510(k) number K013869. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SR IVOCRON?

SR IVOCRON is a medical device that received FDA 510(k) clearance on 2002-08-28. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K013869.

When did SR IVOCRON receive FDA 510(k) clearance?

SR IVOCRON received FDA 510(k) clearance on 2002-08-28, under 510(k) number K013869.

Who is the listed applicant for SR IVOCRON?

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 SR IVOCRON?

The FDA product code for SR IVOCRON is EBG.

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Other records listing Ivoclar Vivadent, Inc. as applicant

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Related Devices (Code: EBG)

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.

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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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