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Pulse Rx 2.0, Pulse Pro Rx 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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