Last synced on 14 November 2025 at 11:06 pm

BioWaveGO RX

Page Type
Cleared 510(K)
510(k) Number
K210202
510(k) Type
Special
Applicant
BioWave Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
30 days
Submission Type
Summary

BioWaveGO RX

Page Type
Cleared 510(K)
510(k) Number
K210202
510(k) Type
Special
Applicant
BioWave Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
30 days
Submission Type
Summary