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513(g) Submission, medical device classification, CDRH, USFDA

freyrsolutions (#193) 785 days ago News 513 g submission medical device classif All https://medicaldevices.freyrsolutions.com   Discuss  Published New Discard Success!

Freyr provides regulatory support for medical device manufacturers in 513 g submission, which includes medical device classification, preparation & review of 513g application and interaction with agency to comply with CDRH, FDA.