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Endoscope, Neurological

FDA product code GWG · 91 cleared devices

Class 2 Neurology
Regulation
21 CFR 882.1480
Review panel
NE
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1992-12-21 – 2026-06-04

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).

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