510(k) K221959
- Device
- Q21
- Applicant
- Neurofield, Inc.
- 510(k) number
- K221959
- Product code
- GWQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2023-08-31
- Date received
- 2022-07-05
- Regulation
- 882.1400
- Classification name
- Full-Montage Standard Electroencephalograph
- Medical specialty
- Neurology
- Review panel
- Neurology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- Nicholas J. Dogris
- Address
- 386 W. Ln. Bishop CA US 93514 93514
FDA Registration Numbers
- 9710602
- 3008857629
- 9680891
- 2430863
- 9681860
- 3027256461
- 3013501110
- 3017666517
- 3019388613
- 3021826057
- 3010157426
- 1531052
- 8022257
- 3006125362
- 3018094310
- 3030154814
- 9615126
- 3018783526
- 3017970307
- 3013757456
- 3003851073
- 3009649442
- 3006315274
- 3021736577
- 3013596024
- 3013500228
- 3013679558
- 9610816
- 3013413442
- 3010900508
- 3007611554
- 3007323246
- 3005550372
- 3005877899
- 3008483389
- 3016852448
- 3006418479
- 3008058135
- 3008881376
- 3038189172
- 1530224
- 9710486
- 1045254
- 8020045
- 3004753785
- 3006177498
- 2023374
- 9612330
- 3020223448
- 3023272766
- 3009831876
- 3013671918
- 3029984080
- 3010762896
- 3004415095
- 3012359877
- 3007701713
- 1651104
- 9612389
- 1063925
- 2518422
- 3015491430
- 3016618143
- 3007962724
- 3008132398
- 3010536822
- 9611252
- 3027532607
- 3029922
- 3011353843
- 9617127
- 3012494290
- 3032109181
- 3011047165
- 3000126629
- 1219324
- 3004883754
- 3023707151
- 9613619
Source Documents
Related GUDID Devices
| Primary DI | Brand | Company | Published |
|---|---|---|---|
| 00860410000379 | Q21 | NEUROFIELD, INC. | 2025-06-02 |
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