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Flowonix Medical Inc

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Prometra Programmable 20mL Pump. Catalog No. 11827 The device is an implantable infusion p recall (Z-1120-2020)Flowonix Medical Inc2020-02-10
Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN- recall (Z-1121-2020)Flowonix Medical Inc2020-02-10
Prometra II 40mL Pump. Catalog No. 16827 The device is an implantable infusion pump. GTIN- recall (Z-1122-2020)Flowonix Medical Inc2020-02-10
US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusio recall (Z-1123-2020)Flowonix Medical Inc2020-02-10
Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion p recall (Z-1124-2020)Flowonix Medical Inc2020-02-10
Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusio recall (Z-1125-2020)Flowonix Medical Inc2020-02-10
PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 1382 recall (Z-2740-2017)Flowonix Medical, Inc.2017-06-19

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Every clearance here is in the API, with alerts when new ones post.