Nihon Kohden Corporation - Eastern Japan Logistics Center
Sakado City Saitama, JP
Nihon Kohden Corporation - Eastern Japan Logistics Center appears in FDA device records in Sakado City Saitama, JP. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3016852448 | 3016852448 | Nihon Kohden Corporation - Eastern Japan Logistics Center | 1-1 Nishi-Inter, 2-Chome, Sakado City Saitama 350-0259 JP | 2026 | and 29 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- DRQAmplifier And Signal Conditioner, Transducer Signal
- OMAAmplitude-Integrated Electroencephalograph
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- BXAAnalyzer, Gas, Water Vapor, Gaseous-Phase
- OMBAutomatic Event Detection Software For Full-Montage Electroencephalograph
- ORTBurst Suppression Detection Software For Electroencephalograph
- BZAConnector, Airway (Extension)
- DSIDetector And Alarm, Arrhythmia
- GZODevice, Galvanic Skin Response Measurement
- JXEDevice, Nerve Conduction Velocity Measurement
- DPSElectrocardiograph
- GYCElectrode, Cortical
- GXYElectrode, Cutaneous
- JJPElectrode, Ion Selective (Non-Specified)
- IKTElectrode, Needle, Diagnostic Electromyograph
- IKNElectromyograph, Diagnostic
- MNKEndoscopic Bite Block
- GWQFull-Montage Standard Electroencephalograph
- KGKGas, Collecting Vessel
- HPPHeadlamp, Operating, Battery-Operated
- GYBMedia, Electroconductive
- KMIMonitor, Bed Patient
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- OLTNon-Normalizing Quantitative Electroencephalograph Software
- HXBProbe
- KAKProbe, Ent
- IZDProbe, Uptake, Nuclear
- OMCReduced- Montage Standard Electroencephalograph
- OLVStandard Polysomnograph With Electroencephalograph
- GWJStimulator, Auditory, Evoked Response
- GWFStimulator, Electrical, Evoked Response
- KOIStimulator, Nerve, Peripheral, Electric
- GWEStimulator, Photic, Evoked Response
- IOYSupport, Arm
- MSXSystem, Network And Communication, Physiological Monitors
- GYATester, Electrode/Lead, Electroencephalograph
- DRGTransmitters And Receivers, Physiological Signal, Radiofrequency
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain