Hello
Hope you're all doing well!
We're a Medical Device Company headquartered in Belgium. Our US locations are Los Angeles and New York.
We have a Software as a Medical Device that we're looking to get 510 (k) Clearance for and have a pretty tight deadline. We're looking for experienced Regulatory Consultants who can help us with this Submission. Kindly shoot me an email at anjali.nair@fluidda.com and we can discuss a proposal.
Kindly let me know when is a good time to talk.
Thanks
Regards,
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Anjali Nair
Los Angeles, CA
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