Planmed OY

20 FDA 510(k) medical device clearances.

Top product codes for Planmed OY

Recent clearances by Planmed OY

K250318 — Planmed XFI SFV · 2025-09-26
K211720 — Planmed Clarity 2D, Planmed Clarify S MUE · 2022-07-18
K213278 — Planmed Verity OAS · 2022-04-28
K192317 — Planmed Clarity 2D and Clarity S MUE · 2020-10-23
K180918 — Planmed Verity OAS · 2018-11-30
K163328 — Planmed Clarity MUE · 2017-12-28
K143435 — Planmed Verity OAS · 2015-05-14
K121418 — PLANMED VERITY JAK · 2013-02-01
K121963 — PLANMED NUANCE DIGIGUIDE MUE · 2012-11-21
K042671 — PLANMED SOPHIE NUANCE CLASSIC IZH · 2004-11-19
K021945 — PLANMED SOPHIE & SOPHIE CLASSIC (WITH DIGISPOT AND CYTOGUIDE) IZH · 2003-02-21
K013656 — PLANMED SOPHIE & PLANMED SOPHIE CLASSIC IZH · 2002-01-16
K010116 — PLANMED SOPHIE, PLANMED SOPHIE CLASSIC IZH · 2001-03-15
K991826 — PLANMED SOPHIE AND SOPHIE CLASSIC IZH · 1999-08-10
K983659 — PLANMED SOPHIE & PLANNED SOPHIE CLASSIC IZH · 1998-11-16
K973493 — PLANMED CYTOGUIDE IZH · 1997-11-10
K962105 — PLANNED SOPHIED CLASSIC IZH · 1997-02-05
K951883 — PLANMED SOPHIE MAMMOGRAPHIC X-RAY UNIT IZH · 1995-05-24
K934373 — MOBILE SOPHIE MODIFICATION IZH · 1994-04-07
K923471 — PLANMED CYTOGUIDE IZH · 1992-11-24

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