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FDA 510(k)

KAVO CORUND HANDPIECE 2013

K-Number: K002708 · 2000-11-28

ApplicantKavo America
Decision Date2000-11-28
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KAVO CORUND HANDPIECE 2013 is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America. It received FDA 510(k) clearance on 2000-11-28 under 510(k) number K002708. 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 KAVO CORUND HANDPIECE 2013?

KAVO CORUND HANDPIECE 2013 is a medical device that received FDA 510(k) clearance on 2000-11-28. The listed applicant is Kavo America. The 510(k) number is K002708.

When did KAVO CORUND HANDPIECE 2013 receive FDA 510(k) clearance?

KAVO CORUND HANDPIECE 2013 received FDA 510(k) clearance on 2000-11-28, under 510(k) number K002708.

Who is the listed applicant for KAVO CORUND HANDPIECE 2013?

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

What is the FDA product code for KAVO CORUND HANDPIECE 2013?

The FDA product code for KAVO CORUND HANDPIECE 2013 is KOJ.

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Other records listing Kavo America 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.

K073074KEY LASER III 1243 US WITH DETECTK072262GENTLERAY 980 DIODE LASER SYSTEMK063624KAVO EVEREST C-TEMPK051909DIAGNODENTK030146KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+K050019IN EXAM INTRAORAL DENTAL X-RAY SYSTEM

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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 GmbHK033215PREPAIRDanville Materials, Inc.K024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, 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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