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FDA 510(k)

PREPAIR

K-Number: K033215 · 2004-01-09

ApplicantDanville Materials, Inc.
Decision Date2004-01-09
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PREPAIR is the device name listed in this FDA 510(k) record. The listed applicant is Danville Materials, Inc.. It received FDA 510(k) clearance on 2004-01-09 under 510(k) number K033215. 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 PREPAIR?

PREPAIR is a medical device that received FDA 510(k) clearance on 2004-01-09. The listed applicant is Danville Materials, Inc.. The 510(k) number is K033215.

When did PREPAIR receive FDA 510(k) clearance?

PREPAIR received FDA 510(k) clearance on 2004-01-09, under 510(k) number K033215.

Who is the listed applicant for PREPAIR?

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

What is the FDA product code for PREPAIR?

The FDA product code for PREPAIR is KOJ.

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Other records listing Danville Materials, Inc. 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.

K121880DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUIDK111876Z BOND, PRELUDE ONEK110642SILJETR SYSTEMK102753TURBO TEMP 3K092912STARFILL 2B HV (HIGH VISCOSITY) ROCKCORE, MODEL: 90838 AND STARFILL 2B LV (LOW VISCOSITY), MODEL: 90150K092319STAR VPS, MODEL 80014-01, FIRST QUATER, MODEL 90649, FIRST HALF, MODEL 89387

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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 GmbHK024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, Inc.K030292GROMAN PREPMASTERGroman, Inc.

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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