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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
K220217
01/26/2022
Normatec 3
NormaTec Industries, LP
K221666
06/08/2022
Normatec Go
NormaTec Industries, LP
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