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FDA 510(k)

4 SEASONS

K-Number: K024094 · 2003-02-14

ApplicantIvoclar Vivadent, Inc.
Decision Date2003-02-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

4 SEASONS 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 2003-02-14 under 510(k) number K024094. 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 4 SEASONS?

4 SEASONS is a medical device that received FDA 510(k) clearance on 2003-02-14. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K024094.

When did 4 SEASONS receive FDA 510(k) clearance?

4 SEASONS received FDA 510(k) clearance on 2003-02-14, under 510(k) number K024094.

Who is the listed applicant for 4 SEASONS?

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 4 SEASONS?

The FDA product code for 4 SEASONS is EBF.

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Other records listing Ivoclar Vivadent, Inc. as applicant

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Related Devices (Code: EBF)

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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