FDA _medical device_Kentron Insight News

List of approved products for the month of march 2020

All medical device manufacturer apply for FDA approval to be legally marketed in the USA. The medical device of belonging to class I, II and III moves through the 510K approval process and class III goes through PMA premarket approval process

Here is the list of 510K and PMA products for the month of March 2020

We product details intelligence service of each product for medical and pharmaceutical sector.

Posted in Medical Device and tagged .

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