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AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022681
510(k) Type
Traditional
Applicant
Azog, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2002
Days to Decision
81 days
Submission Type
Summary

AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022681
510(k) Type
Traditional
Applicant
Azog, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2002
Days to Decision
81 days
Submission Type
Summary