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Electromyograph, Diagnostic
FDA product code IKN · Class 2 · Physical Medicine
742
Registered devices
111
Adverse events
1
Recalls
75
510(k) clearances
Devices with this code
Sierra Summit — CADWELL INDUSTRIES, INC.NATUS NEUROLOGY — NATUS NEUROLOGY INCORPORATEDGuidance — Nuvasive, Inc.NA — MEDTRONIC XOMED, INC.NVJJB — Nuvasive, Inc.Cascade Elite — CADWELL INDUSTRIES, INC.IOMAX Extender Pod — CADWELL INDUSTRIES, INC.PULSE — Nuvasive, Inc.EPAD — SAFEOP SURGICAL, INC.NVM5 — Nuvasive, Inc.NVM5 — Nuvasive, Inc.NA — NIHON KOHDEN CORPORATIONSierra Summit — CADWELL INDUSTRIES, INC.SafeOp — ALPHATEC SPINE, INC.Sierra Wave — CADWELL INDUSTRIES, INC.MyoVision Wirefree System — PRECISION BIOMETRICS INCNA — MEDTRONIC XOMED, INC.PULSE — Nuvasive, Inc.Remote Monitoring — Nuvasive, Inc.Power-LAN Connection Box — EB NEURO SPANatus — XLTEKPULSE — Nuvasive, Inc.K7 Evaluation System-CMS — MYOTRONICS NOROMED, INCPULSE — Nuvasive, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-01-29 | SpineMatrix Inc | A full design review of the CERSR system was conducted in 7/2009. The audit revealed numerous design verification tests that either did not pass or did not mee |
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