Electromek Diagnostic Systems, Inc.
FDA 510(k) medical device clearances.
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.