JETPOLISHER
K-Number: K014249 · 2002-02-19
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Device Summary
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
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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