GWG — Endoscope, Neurological

21 CFR 882.1480

Class 2

Definition

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Medical Specialty

NE

Review Panel

NE

Submission Type

1

FDA Authorisations (91)

Device Name K-Number
HJY VisualNext 3D Endoscopic Vision System K243429
AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80) K250752
cCeLL - In vivo K233391
Digital ClarusScope System, Digital NeuroPEN System K223615
Aurora Surgiscope System K232618
Neuroblade System K230125
QEVO System K232159
HJY VisualNext Endoscopic Vision System K222735
1688 4K Camera System, L11 LED Light Source with AIM, AIM SafeLight Cable, Precision S 4K Sinuscopes K211202
ClearPath Disposable Introducer K210251
Clarus Peel-Away Introducer Sheath K200925
Axonpen, Axonmonitor, Axonbox, Tablet K201308
Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) K201840
Aurora Surgiscope System K191861
Artemis Eye System K190719
Aurora Surgiscope System K182211
MR Compatible Aspiration Kit K181731
CONVIVO K181116
Cellvizio 100 Series Systems with Confocal Miniprobes K180270
KARL STORZ ICG Imaging System K180146
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