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Flowflex® Plus COVID-19 Home Test

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233373
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
200 days
Submission Type
Statement

Flowflex® Plus COVID-19 Home Test

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233373
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
200 days
Submission Type
Statement