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Pulse Rx 2.0, Pulse Pro Rx 2.0

Page Type
Cleared 510(K)
510(k) Number
K183328
510(k) Type
Traditional
Applicant
NormaTec Industries, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2018
Days to Decision
21 days
Submission Type
Summary

Pulse Rx 2.0, Pulse Pro Rx 2.0

Page Type
Cleared 510(K)
510(k) Number
K183328
510(k) Type
Traditional
Applicant
NormaTec Industries, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2018
Days to Decision
21 days
Submission Type
Summary