Electromek Diagnostic Systems, Inc.
Electromek Diagnostic Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1991.
Top product codes for Electromek Diagnostic Systems, Inc.
Recent clearances by Electromek Diagnostic Systems, Inc.
- K902986 — G.E. DXD 325/350/350II/DXD 525/525II GENERATORS
- K902987 — G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS
- K902985 — G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN
- K902988 — G.E. MSI 850/850II/1250 THREE PHASE GENERATORS
- K902982 — G.E. POLARIX II C-ARM
- K902981 — G.E. FLUOROCON 300 IMAGING SYSTEM
- K902983 — SIEMEN'S SIREMOBILE II C-ARM
- K902791 — G.E. 48-4 CEILING TUBEHANGER
- K902989 — G.E. MONITROL 90 AND G.E. MONITROL 15
- K902984 — G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS
- K902980 — G.E. XT CEILING TUBE SUSPENSION
Data sourced from openFDA. This site is unofficial and independent of the FDA.