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FDA 510(k)

PAINT- ON POLISH AGENT

K-Number: K070306 · 2007-03-22

Decision Date2007-03-22
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PAINT- ON POLISH AGENT is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International, Inc.. It received FDA 510(k) clearance on 2007-03-22 under 510(k) number K070306. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAINT- ON POLISH AGENT?

PAINT- ON POLISH AGENT is a medical device that received FDA 510(k) clearance on 2007-03-22. The listed applicant is Dentsply International, Inc.. The 510(k) number is K070306.

When did PAINT- ON POLISH AGENT receive FDA 510(k) clearance?

PAINT- ON POLISH AGENT received FDA 510(k) clearance on 2007-03-22, under 510(k) number K070306.

Who is the listed applicant for PAINT- ON POLISH AGENT?

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

What is the FDA product code for PAINT- ON POLISH AGENT?

The FDA product code for PAINT- ON POLISH AGENT is EBD.

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 Dentsply International, Inc. 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.

View all 31 devices →

Related Devices (Code: EBD)

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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