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Re: IPwatcher post# 86734

Saturday, 06/20/2020 9:35:40 PM

Saturday, June 20, 2020 9:35:40 PM

Post# of 97213

So it looks like GenAccord may simple be a reboxing of an HMD Biomedical Inc. product line?



Looks like HMD had an FDA warning letter in 2017.
They got a 510K approval in 2019 so I would assume that they probably got out from under this OK however.

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/hmd-biomedical-inc-499698-08312016

You can see all their device listings by typing HMD biomedical into the applicant name box on this search from from the FDA website.
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm

K121433 or K113314 seem closest in intended use to DECNs Genaccord published information from what I can see. But there is a degree of speculation in there.

It seems unlikely that the FDA cleared 'GenAccord' was developed by DECN themselves though. Pharmatech website suggests it is a rebadged HMD Biomedical product

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