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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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Z-0590-04 - Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001096-1 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
Z-0591-04 - Cronus Endovascular Guidewire, Length 210 cm (partial coat), Diameter 0.014 inch, Part Number 001-001096-3 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
Z-0595-04 - Cronus-1 Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001263-1 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
Z-0593-04 - Floppy Cronus Endovascular Guidewire, Length 180 cm (partial coat), Diameter 0.014 inch, Part Number 001-001232-3 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
Z-0594-04 - Floppy Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, Part Number 001-001232-4 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
Z-0592-04 - Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, Part Number 001-001096-4 2 07/20/2004 FEI # 3003084417
Stereotaxis Inc
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