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FAQ™ 201, FAQ™ 202

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240378
510(k) Type
Traditional
Applicant
Foreo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
72 days
Submission Type
Statement

FAQ™ 201, FAQ™ 202

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240378
510(k) Type
Traditional
Applicant
Foreo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
72 days
Submission Type
Statement