FDWClass II
Esophagoscope, Rigid, Gastro-urology
Gastroenterology, Urology · 21 CFR 876.1500
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).
MDR events1All time
Recalls0All time
Registered firms0Currently listed
510(k) clearances0All time
Recent MDR events
1 adverse event reports on file
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
0 firms currently registered for this product code
No registered firms found for this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.