Last synced on 14 November 2025 at 11:06 pm

PressOn Electrode Headset

Page Type
Cleared 510(K)
510(k) Number
K190801
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
103 days
Submission Type
Summary

PressOn Electrode Headset

Page Type
Cleared 510(K)
510(k) Number
K190801
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
103 days
Submission Type
Summary