Planmeca Viso— 510(k) K230985

Substantially Equivalent

Planmeca Oy

FDA 510(k) clearance K230985 for Planmeca Viso, Substantially Equivalent on 2023-12-28. Applicant: Planmeca Oy.

Clearance details

Applicant: Planmeca Oy
Product code: Code OAS
Advisory panel: Radiology
Date received: 2023-04-06
Decision date: 2023-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, FI

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