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FDA 510(k)

SANDBLASTER

K-Number: K931845 · 1995-03-01

ApplicantMirage Dental Systems
Decision Date1995-03-01
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SANDBLASTER is the device name listed in this FDA 510(k) record. The listed applicant is Mirage Dental Systems. It received FDA 510(k) clearance on 1995-03-01 under 510(k) number K931845. 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 SANDBLASTER?

SANDBLASTER is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Mirage Dental Systems. The 510(k) number is K931845.

When did SANDBLASTER receive FDA 510(k) clearance?

SANDBLASTER received FDA 510(k) clearance on 1995-03-01, under 510(k) number K931845.

Who is the listed applicant for SANDBLASTER?

The FDA 510(k) record lists Mirage Dental Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SANDBLASTER?

The FDA product code for SANDBLASTER is KOJ.

Related Clinical Trials

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Other records listing Mirage Dental Systems 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.

K923895QUIKSEALK915511MIRAGE COMPLETE KIT AND MIRAGE ABC KIT

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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