Armory Motion— 510(k) K213097

Name: FDA 510(k) clearance K213097
Creator: U.S. Food and Drug Administration
Published: 2022-06-10

Substantially Equivalent

Pain Management Technologies, Inc.

FDA 510(k) clearance K213097 for Armory Motion, Substantially Equivalent on 2022-06-10. Applicant: Pain Management Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Pain Management Technologies, Inc.
Product code: Code ILO
Device class: Class 2
Regulation: 21 CFR 890.5720
Advisory panel: Physical Medicine
Date received: 2021-09-24
Decision date: 2022-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

Download summary PDF View on FDA.gov ↗

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