ImmersiveView Surgical Plan (IVSP®)— 510(k) K181813

Name: FDA 510(k) clearance K181813
Creator: U.S. Food and Drug Administration
Published: 2020-06-09

Substantially Equivalent

Immersivetouch

FDA 510(k) clearance K181813 for ImmersiveView Surgical Plan (IVSP®), Substantially Equivalent on 2020-06-09. Applicant: Immersivetouch. Device class: 2.

Clearance details

Applicant: Immersivetouch
Product code: Code DZJ
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2018-07-06
Decision date: 2020-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westmont, IL, US

Download summary PDF View on FDA.gov ↗

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