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Electromyograph, Diagnostic
FDA product code IKN · Class 2 · Physical Medicine
743
Registered devices
111
Adverse events
1
Recalls
75
510(k) clearances
Devices with this code
NVM5 — Nuvasive, Inc.NATUS NEUROLOGY — NATUS NEUROLOGY INCORPORATEDPULSE — Nuvasive, Inc.NVM5 — Nuvasive, Inc.NA — Nuvasive, Inc.EPAD — SAFEOP SURGICAL, INC.PULSE — Nuvasive, Inc.N/A — MEDTRONIC SOFAMOR DANEK, INC.NA — NIHON KOHDEN AMERICA, INC.PULSE — Nuvasive, Inc.EPAD — SAFEOP SURGICAL, INC.MyoVision Software — PRECISION BIOMETRICS INCPULSE — Nuvasive, Inc.NA — MEDTRONIC XOMED, INC.Sierra Summit — CADWELL INDUSTRIES, INC.PULSE — Nuvasive, Inc.Nexstim Head Tracker Tape — Nexstim OyjQuickScan Pads — PRECISION BIOMETRICS INCBendini — Nuvasive, Inc.MyoVision Software — PRECISION BIOMETRICS INCNeuropack S3 — NIHON KOHDEN AMERICA, INC.NATUS NEUROLOGY — NATUS NEUROLOGY INCORPORATEDPULSE — Nuvasive, Inc.PULSE — 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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