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FDA submission w/ 510k assistance

Professional Service

RAC Corp offers a high-level approach for assistance in regulatory compliance and product analysis. RAC Corp aids in the process for your medical device regulatory submissions in the US and overseas for the following:   FDA clearance (510(k)), FDA Establishment Registration and Product Listing, CE Marking, and Import/Export Requirements.

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For sales inquiries regarding our FDA submission w/ 510k assistance service, please call 9494126689, email mcarden@raccorp.net, or use the form below.