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 the device name listed in this FDA 510(k) record. The listed applicant is Pain Management Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-10 under 510(k) 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. The listed applicant is Pain Management Technologies, Inc.. The 510(k) number is K213097.
When did Armory Motion receive FDA 510(k) clearance?
Armory Motion received FDA 510(k) clearance on 2022-06-10, under 510(k) number K213097.
Who is the listed applicant for Armory Motion?
The FDA 510(k) record lists Pain Management Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.