Release #:812-187714-rl-1235735: Orthopedic Desig
Post# of 7805
Orthopedic Design & Technology
BioElectronics Corporation
ActiPatch Achieves FDA Market Clearance
BioElectronics Corporation, the maker of non-invasive electroceutical devices, has obtained a new 510(k) clearance from the U.S. Food and Drug Administration (FDA). This over-the counter marketing clearance was granted for the drug free ActiPatch medical device, for the indication: “adjunctive treatment of musculoskeletal pain.”
The ActiPatch was already FDA-cleared for over-the-counter treatment of pain from knee osteoarthritis and plantar fasciitis (heel pain) in 2017. The latest clearance expands these indications to cover all musculoskeletal pain complaint ...
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2/24/2020 6:08:44 AM