Planmed OY
Planmed OY holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2025.
Top product codes for Planmed OY
Recent clearances by Planmed OY
- K250318 — Planmed XFI
- K211720 — Planmed Clarity 2D, Planmed Clarify S
- K213278 — Planmed Verity
- K192317 — Planmed Clarity 2D and Clarity S
- K180918 — Planmed Verity
- K163328 — Planmed Clarity
- K143435 — Planmed Verity
- K121418 — PLANMED VERITY
- K121963 — PLANMED NUANCE DIGIGUIDE
- K042671 — PLANMED SOPHIE NUANCE CLASSIC
- K021945 — PLANMED SOPHIE & SOPHIE CLASSIC (WITH DIGISPOT AND CYTOGUIDE)
- K013656 — PLANMED SOPHIE & PLANMED SOPHIE CLASSIC
- K010116 — PLANMED SOPHIE, PLANMED SOPHIE CLASSIC
- K991826 — PLANMED SOPHIE AND SOPHIE CLASSIC
- K983659 — PLANMED SOPHIE & PLANNED SOPHIE CLASSIC
- K973493 — PLANMED CYTOGUIDE
- K962105 — PLANNED SOPHIED CLASSIC
- K951883 — PLANMED SOPHIE MAMMOGRAPHIC X-RAY UNIT
- K934373 — MOBILE SOPHIE MODIFICATION
- K923471 — PLANMED CYTOGUIDE
Data sourced from openFDA. This site is unofficial and independent of the FDA.