Minn. lawmakers air concerns over possible changes to 510(k) process

05/27/2010 | Pioneer Press (St. Paul, Minn.)

Sen. Amy Klobuchar, D-Minn., and Rep. Erik Paulsen, R-Minn., sent a letter to the FDA saying the proposed changes to the 510(k) process would stifle medical device innovation and result in unnecessary regulations for companies. Minnesota houses more than 400 medical-device firms that provide jobs for more than 50,000 people.

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Pioneer Press (St. Paul, Minn.)

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