Last synced on 14 November 2025 at 11:06 pm

RelieVRx (Pico G3)

Page Type
Cleared 510(K)
510(k) Number
K251519
510(k) Type
Traditional
Applicant
AppliedVR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2025
Days to Decision
89 days
Submission Type
Summary

RelieVRx (Pico G3)

Page Type
Cleared 510(K)
510(k) Number
K251519
510(k) Type
Traditional
Applicant
AppliedVR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2025
Days to Decision
89 days
Submission Type
Summary