Medical Device Recalls
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61 to 70 of 79 Results
510(K) Number: K113501 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen 8 Panel Dip Card, Item No. PSD-8P ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300 ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W ... | 3 | 12/24/2015 | Ameditech Inc |
ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W ... | 3 | 12/24/2015 | Ameditech Inc |
RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA ... | 3 | 12/24/2015 | Ameditech Inc |
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
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