Last synced on 16 May 2025 at 11:05 pm

NormaTec Pulse and NormaTec Pulse Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160608
510(k) Type
Traditional
Applicant
NORMATEC INDUSTRIES, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2016
Days to Decision
41 days
Submission Type
Summary

NormaTec Pulse and NormaTec Pulse Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160608
510(k) Type
Traditional
Applicant
NORMATEC INDUSTRIES, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2016
Days to Decision
41 days
Submission Type
Summary