EM-07 Cordless Endo Motor— 510(k) K232551

Name: FDA 510(k) clearance K232551
Creator: U.S. Food and Drug Administration
Published: 2024-07-09

Substantially Equivalent

Forum Engineering Technologies (96) , Ltd.

FDA 510(k) clearance K232551 for EM-07 Cordless Endo Motor, Substantially Equivalent on 2024-07-09. Applicant: Forum Engineering Technologies (96) , Ltd.. Device class: 1.

Clearance details

Applicant: Forum Engineering Technologies (96) , Ltd.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2023-08-23
Decision date: 2024-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ashkelon, IL

Download summary PDF View on FDA.gov ↗

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