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Electromek Diagnostic Systems, Inc.

11 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
G.E. DXD 325/350/350II/DXD 525/525II GENERATORS (K902986)Electromek Diagnostic Systems, Inc.1991-02-13
G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS (K902987)Electromek Diagnostic Systems, Inc.1990-12-26
G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN (K902985)Electromek Diagnostic Systems, Inc.1990-12-19
G.E. MSI 850/850II/1250 THREE PHASE GENERATORS (K902988)Electromek Diagnostic Systems, Inc.1990-12-19
G.E. POLARIX II C-ARM (K902982)Electromek Diagnostic Systems, Inc.1990-11-13
G.E. FLUOROCON 300 IMAGING SYSTEM (K902981)Electromek Diagnostic Systems, Inc.1990-11-07
SIEMEN'S SIREMOBILE II C-ARM (K902983)Electromek Diagnostic Systems, Inc.1990-11-06
G.E. 48-4 CEILING TUBEHANGER (K902791)Electromek Diagnostic Systems, Inc.1990-10-29
G.E. MONITROL 90 AND G.E. MONITROL 15 (K902989)Electromek Diagnostic Systems, Inc.1990-10-29
G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS (K902984)Electromek Diagnostic Systems, Inc.1990-10-26
G.E. XT CEILING TUBE SUSPENSION (K902980)Electromek Diagnostic Systems, Inc.1990-10-23

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