Planmeca ProMax 3D Max, Planmeca Maximity— 510(k) K160506

Substantially Equivalent

Planmeca Oy

FDA 510(k) clearance K160506 for Planmeca ProMax 3D Max, Planmeca Maximity, Substantially Equivalent on 2016-05-20. Applicant: Planmeca Oy.

Clearance details

Applicant
Planmeca Oy
Product code
Code OAS
Advisory panel
Radiology
Date received
Decision date
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.