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Seismed Instruments, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K910994 MODIFIED SEISMOCARDIOGRAPHDSB1992-01-15 View
510(k) K900130 MODIFIED SEISMOCARDIOGRAPHDSB1990-03-28 View
510(k) K892323 SEISMOCARDIOGRAPH - SCG(TM) 1000 SERIESDSB1989-10-30 View
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