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FDA 510(k)

JETPOLISHER

K-Number: K014249 · 2002-02-19

Decision Date2002-02-19
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JETPOLISHER is the device name listed in this FDA 510(k) record. The listed applicant is Deldent , Ltd.. It received FDA 510(k) clearance on 2002-02-19 under 510(k) number K014249. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JETPOLISHER?

JETPOLISHER is a medical device that received FDA 510(k) clearance on 2002-02-19. The listed applicant is Deldent , Ltd.. The 510(k) number is K014249.

When did JETPOLISHER receive FDA 510(k) clearance?

JETPOLISHER received FDA 510(k) clearance on 2002-02-19, under 510(k) number K014249.

Who is the listed applicant for JETPOLISHER?

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

What is the FDA product code for JETPOLISHER?

The FDA product code for JETPOLISHER is KOJ.

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 Deldent , Ltd. 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: KOJ)

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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