DELIGHT— 510(k) K923462

Substantially Equivalent

Planmeca USA, Inc.

FDA 510(k) clearance K923462 for DELIGHT, Substantially Equivalent on 1992-12-21. Applicant: Planmeca USA, Inc.. Device class: 1.

Clearance details

Applicant: Planmeca USA, Inc.
Product code: Code EAZ
Device class: Class 1
Regulation: 21 CFR 872.4630
Advisory panel: Dental
Date received: 1992-07-14
Decision date: 1992-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Finland, FI

Download summary PDF View on FDA.gov ↗

Recent devices under product code EAZ

K072309 — MICROLUX/BLU2007-11-19
K041614 — MICROLUX DL2005-04-04
K033033 — VIZILITE-BLUE ORAL EXAM KIT2004-11-22
K003995 — SPECULITE/ORALLITE2001-03-16
K926081 — DENTAL LIGHT1994-01-26

More clearances from Planmeca USA, Inc.

K111361 — PLANMED NUANCE EXCEL2011-09-23
K081699 — PLANMECA SOVEREIGN2008-08-29
K923534 — PM2002 PROLINE1994-01-31
K923533 — ADMARK1993-03-04
K923461 — PM2002 PROLINE, PM2002 PROLINE EC1992-12-21

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