FEB · Class II · 21 CFR 876.1500

FDA Product Code FEB: Accessories, Cleaning, For Endoscope

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).

Leading manufacturers include STERIS Corporation and Wassenburg Medical, Inc..

57
Total
57
Cleared
209d
Avg days
1981
Since
57 devices
49–57 of 57
No devices found for this product code.