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Theradome LH80 PRO

Page Type
Cleared 510(K)
510(k) Number
K171775
510(k) Type
Traditional
Applicant
Theradome Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
209 days
Submission Type
Summary

Theradome LH80 PRO

Page Type
Cleared 510(K)
510(k) Number
K171775
510(k) Type
Traditional
Applicant
Theradome Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
209 days
Submission Type
Summary