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U.S. Department of Health and Human Services

Medical Device Recalls
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81 to 84 of 84 Results
510(K) Number: K052115
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ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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