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FDA 510(k)

LIGHT TIP

K-Number: K022265 · 2002-10-02

Decision Date2002-10-02
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT TIP is the device name listed in this FDA 510(k) record. The listed applicant is Svenska Dental Instruments AB. It received FDA 510(k) clearance on 2002-10-02 under 510(k) number K022265. 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 LIGHT TIP?

LIGHT TIP is a medical device that received FDA 510(k) clearance on 2002-10-02. The listed applicant is Svenska Dental Instruments AB. The 510(k) number is K022265.

When did LIGHT TIP receive FDA 510(k) clearance?

LIGHT TIP received FDA 510(k) clearance on 2002-10-02, under 510(k) number K022265.

Who is the listed applicant for LIGHT TIP?

The FDA 510(k) record lists Svenska Dental Instruments AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHT TIP?

The FDA product code for LIGHT TIP is EBZ.

Related Clinical Trials

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.

Other records listing Svenska Dental Instruments AB as applicant

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.

Related Devices (Code: EBZ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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