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PulseRelief

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151035
510(k) Type
Traditional
Applicant
Philips Consumer Lifestyle
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2015
Days to Decision
95 days
Submission Type
Summary

PulseRelief

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151035
510(k) Type
Traditional
Applicant
Philips Consumer Lifestyle
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2015
Days to Decision
95 days
Submission Type
Summary