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FDA 510(k)

JETSONIC 2000

K-Number: K014245 · 2002-01-29

ApplicantDeldent , Ltd.
Decision Date2002-01-29
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JETSONIC 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Deldent , Ltd.. It received FDA 510(k) clearance on 2002-01-29 under 510(k) number K014245. 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 JETSONIC 2000?

JETSONIC 2000 is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is Deldent , Ltd.. The 510(k) number is K014245.

When did JETSONIC 2000 receive FDA 510(k) clearance?

JETSONIC 2000 received FDA 510(k) clearance on 2002-01-29, under 510(k) number K014245.

Who is the listed applicant for JETSONIC 2000?

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 JETSONIC 2000?

The FDA product code for JETSONIC 2000 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.

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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.

K014249JETPOLISHERK014252JETSTREAMK014238DELSONIC 2000K013969MINIBLASTERK011179DELDENT ULTRASONIC INSERTS

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.

K251425turbodent touchMectron S.P.A.K063236BETA-POWDERBrainbase CorporationK042872RONDOFLEX PLUS 360Kavo America CorporationK033675PROSMILE AIR POLISHER AND PROPHYLAXIS POWDERSirona Dental Systems GmbHK033215PREPAIRDanville Materials, Inc.K024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, Inc.

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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