Last synced on 14 November 2025 at 11:06 pm

GyroStim

Page Type
Cleared 510(K)
510(k) Number
K220231
510(k) Type
Traditional
Applicant
UltraThera Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2022
Days to Decision
90 days
Submission Type
Summary

GyroStim

Page Type
Cleared 510(K)
510(k) Number
K220231
510(k) Type
Traditional
Applicant
UltraThera Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2022
Days to Decision
90 days
Submission Type
Summary