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ACON QUIK-CHECK II MIDSTREAM HOME PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032510
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2003
Days to Decision
39 days
Submission Type
Summary

ACON QUIK-CHECK II MIDSTREAM HOME PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032510
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2003
Days to Decision
39 days
Submission Type
Summary