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FDA 510(k)

MINIBLASTER

K-Number: K013969 · 2002-01-10

ApplicantDeldent , Ltd.
Decision Date2002-01-10
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINIBLASTER is the device name listed in this FDA 510(k) record. The listed applicant is Deldent , Ltd.. It received FDA 510(k) clearance on 2002-01-10 under 510(k) number K013969. 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 MINIBLASTER?

MINIBLASTER is a medical device that received FDA 510(k) clearance on 2002-01-10. The listed applicant is Deldent , Ltd.. The 510(k) number is K013969.

When did MINIBLASTER receive FDA 510(k) clearance?

MINIBLASTER received FDA 510(k) clearance on 2002-01-10, under 510(k) number K013969.

Who is the listed applicant for MINIBLASTER?

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 MINIBLASTER?

The FDA product code for MINIBLASTER is KOJ.

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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.

K014249JETPOLISHERK014252JETSTREAMK014245JETSONIC 2000K014238DELSONIC 2000K011179DELDENT 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.

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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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