FDA 510(k) Applications Submitted by NORMATEC INDUSTRIES, LP

FDA 510(k) Number Submission Date Device Name Applicant
K183169 11/16/2018 Pulse 2.0, Pulse Pro 2.0 NormaTec Industries, LP
K183328 11/30/2018 Pulse Rx 2.0, Pulse Pro Rx 2.0 NormaTec Industries, LP
K112890 09/30/2011 NORMATEC MVP NORMATEC INDUSTRIES, LP
K160608 03/03/2016 NormaTec Pulse and NormaTec Pulse Pro NORMATEC INDUSTRIES, LP
K161346 05/16/2016 NormaTec PCD-T and PCD-B NormaTec Industries, LP
K240122 01/16/2024 Normatec Elite NormaTec Industries, LP
K220217 01/26/2022 Normatec 3 NormaTec Industries, LP
K221666 06/08/2022 Normatec Go NormaTec Industries, LP


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