KAVO CORUND HANDPIECE 2013— 510(k) K002708

Substantially Equivalent

Kavo America

FDA 510(k) clearance K002708 for KAVO CORUND HANDPIECE 2013, Substantially Equivalent on 2000-11-28. Applicant: Kavo America. Device class: 2.

Clearance details

Applicant: Kavo America
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 2000-08-30
Decision date: 2000-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Zurich, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KOJ

K251425 — turbodent touch2025-05-09
K063236 — BETA-POWDER2007-02-16
K042872 — RONDOFLEX PLUS 3602004-11-23
K033675 — PROSMILE AIR POLISHER AND PROPHYLAXIS POWDER2004-01-15
K033215 — PREPAIR2004-01-09

More clearances from Kavo America

K073074 — KEY LASER III 1243 US WITH DETECT2008-07-10
K072262 — GENTLERAY 980 DIODE LASER SYSTEM2007-10-26
K063624 — KAVO EVEREST C-TEMP2007-02-08
K051909 — DIAGNODENT2005-10-21
K030146 — KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+2005-08-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.