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Michigan Instruments, Inc.

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000. recall (Z-0178-2007)Michigan Instruments, Inc.2006-11-14
Michigan Instruments Thumper Mechanical CPR Device; Model 1007. recall (Z-0119-2007)Michigan Instruments, Inc.2006-11-03

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