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Distinct® Early Detection Pregnancy Test

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193318
510(k) Type
Traditional
Applicant
Acon Laboratories Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2020
Days to Decision
262 days
Submission Type
Summary

Distinct® Early Detection Pregnancy Test

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193318
510(k) Type
Traditional
Applicant
Acon Laboratories Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2020
Days to Decision
262 days
Submission Type
Summary