AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)— 510(k) K022681

Substantially Equivalent

Azog, Inc.

FDA 510(k) clearance K022681 for AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE), Substantially Equivalent on 2002-11-01. Applicant: Azog, Inc..

Clearance details

Applicant: Azog, Inc.
Product code: Code DHA
Advisory panel: Clinical Chemistry
Date received: 2002-08-12
Decision date: 2002-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phillipsburg, NJ, US

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Adverse events under product code DHA

product code DHA

Malfunction: 1,242
Total: 1,242

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.