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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K032563
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FDA Recall
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In vitro Diagnostic-Clinitest hCG Cassette Pregnancy Test, Radio immunoassay for Human Chorionic Gon... 2 09/01/2008 FEI # 3002637618
Siemens Medical Solutions Diagnostics
Siemens CLINITEST hCG -Pregnancy Test (qualitative), Radio immunoassay,Human Chorionic Gonadotropin ... 2 02/07/2012 FEI # 2432235
Siemens Healthcare Diagnostics
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