Armory Motion
K-Number: K213097 · 2022-06-10
ApplicantPain Management Technologies, Inc.
Decision Date2022-06-10
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Armory Motion is a medical device manufactured by Pain Management Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-10 under approval number K213097. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Armory Motion?
Armory Motion is a medical device that received FDA 510(k) clearance on 2022-06-10. It is manufactured by Pain Management Technologies, Inc.. The 510(k) number is K213097.
When was Armory Motion approved by the FDA?
Armory Motion received FDA 510(k) clearance on 2022-06-10, under approval number K213097.
What company makes Armory Motion?
Armory Motion is manufactured by Pain Management Technologies, Inc..
What is the FDA product code for Armory Motion?
The FDA product code for Armory Motion is ILO.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.