Home / 510(k) Clearances / K984013

510(k) K984013

PLANMECA INTRACAM STATION by Planmeca Oy — Product Code EIA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1999
Date Received
November 11, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Operative Dental
Device Class
Class I
Regulation Number
872.6640
Review Panel
DE
Submission Type

Other clearances by Planmeca Oy

  • K230985 — Planmeca Viso (December 28, 2023)
  • K200572 — Planmeca Romexis (December 2, 2020)
  • K181576 — Planmeca Viso (September 13, 2018)
  • K171385 — Planmeca Romexis (November 14, 2017)
  • K160506 — Planmeca ProMax 3D Max, Planmeca Maximity (May 20, 2016)
  • K140713 — PLANMECA ROMEXIS (June 16, 2014)
  • K103689 — PLANMECA PROMAX 3D MID (March 17, 2011)
  • K093590 — PLANMECA PROMAX 3D MAX (May 12, 2010)
  • K091197 — PLANMECA PROSENSOR (July 29, 2009)
  • K072244 — PLANMECA PROONE (September 21, 2007)

Other clearances for product code EIA

  • K251626 — Midmark Dental Delivery System (November 3, 2025)
  • K251491 — K5 Cart, K5 Mount, K5 Swing (July 17, 2025)
  • K243130 — Integral Dental Unit (June 27, 2025)
  • K242611 — Integral Dental Units (May 27, 2025)
  • K250473 — Dental Delivery System Series 5 and Dental Delivery System Series 5 Plus (February 19, 2025)
  • K242404 — BDC Dental Unit (February 7, 2025)
  • K231297 — Firstar Dental Unit (January 27, 2025)
  • K233805 — K5 (September 3, 2024)
  • K240754 — N2 (March 21, 2024)
  • K231845 — Dental unit Model: Mare (February 28, 2024)