Patient Positioning System— 510(k) K170502

Name: FDA 510(k) clearance K170502
Creator: U.S. Food and Drug Administration
Published: 2017-04-13

Substantially Equivalent

Forte Automation Systems, Inc.

FDA 510(k) clearance K170502 for Patient Positioning System, Substantially Equivalent on 2017-04-13. Applicant: Forte Automation Systems, Inc.. Device class: 2.

Clearance details

Applicant: Forte Automation Systems, Inc.
Product code: Code JAI
Device class: Class 2
Regulation: 21 CFR 892.5770
Advisory panel: Radiology
Date received: 2017-02-21
Decision date: 2017-04-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Machesney Park, IL, US

Download summary PDF View on FDA.gov ↗

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