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Mortara Instrument, Inc

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel recall (Z-1796-2015)Mortara Instrument, Inc2015-06-12
Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated recall (Z-0110-2015)Mortara Instrument, Inc2014-10-22

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