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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
510(K) Number: K880641
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Product Description
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Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST 1 12/08/2022 Remel Inc
Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
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