Orthopantomograph OP 3D LX— 510(k) K230505

Substantially Equivalent

Palodex Group OY

FDA 510(k) clearance K230505 for Orthopantomograph OP 3D LX, Substantially Equivalent on 2023-06-09. Applicant: Palodex Group OY.

Clearance details

Applicant: Palodex Group OY
Product code: Code OAS
Advisory panel: Radiology
Date received: 2023-02-24
Decision date: 2023-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tuusula, FI

Download summary PDF View on FDA.gov ↗

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