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Posted On: 08/09/2021 7:38:39 PM
Post# of 8391
Re: normal_investor #4175
If it were only that simple .......
'Hand-held deep-tissue electromagnetic stimulator' is a standard FDA/GUDID broad category term.
It shows up in documents related to the KT Tape Wave, a PQY Wearable Device.
https://fda.report/GUDID/00851329005463
It shows up in documents related to ActiPatch, a PQY Wearable Device.
https://fda.report/GUDID/00851329005241
It shows up in the Systematized Nomenclature of Medicine code 700548002.
https://www.findacode.com/snomed/700548002--h...lator.html
'Hand-held deep-tissue electromagnetic stimulator' is a standard FDA/GUDID broad category term.
It shows up in documents related to the KT Tape Wave, a PQY Wearable Device.
https://fda.report/GUDID/00851329005463
It shows up in documents related to ActiPatch, a PQY Wearable Device.
https://fda.report/GUDID/00851329005241
It shows up in the Systematized Nomenclature of Medicine code 700548002.
https://www.findacode.com/snomed/700548002--h...lator.html
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