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Electromek Diagnostic Systems, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K902986 G.E. DXD 325/350/350II/DXD 525/525II GENERATORSIZO1991-02-13 View
510(k) K902987 G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORSIZO1990-12-26 View
510(k) K902988 G.E. MSI 850/850II/1250 THREE PHASE GENERATORSIZO1990-12-19 View
510(k) K902985 G.E. MST 625/625II/MST 1050/1050II THREE PHASE GENIZO1990-12-19 View
510(k) K902982 G.E. POLARIX II C-ARMJAA1990-11-13 View
510(k) K902981 G.E. FLUOROCON 300 IMAGING SYSTEMJAA1990-11-07 View
510(k) K902983 SIEMEN'S SIREMOBILE II C-ARMJAA1990-11-06 View
510(k) K902989 G.E. MONITROL 90 AND G.E. MONITROL 15IXR1990-10-29 View
510(k) K902791 G.E. 48-4 CEILING TUBEHANGERKPR1990-10-29 View
510(k) K902984 G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITSIZL1990-10-26 View
510(k) K902980 G.E. XT CEILING TUBE SUSPENSIONJAA1990-10-23 View
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