NLW · Class II · 21 CFR 876.4300

FDA Product Code NLW: Electrode, Electrosurgical, Active, Urological, Reprocessed

The "electrode, Electrosurgical, Active, Urological, Reprocessed" Is Intended To Be Used Endoscopically To Contact Urologic Tissue So As To Allow Cutting, Coagulation, Electrodesiccation, Or Cautery Dessication By Means Of Electric Current. This Device Is Indicated For Reuse/reprocessing. Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.pdf) Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.pdf)

1
Total
1
Cleared
184d
Avg days
2002
Since

FDA 510(k) Cleared Electrode, Electrosurgical, Active, Urological, Reprocessed Devices (Product Code NLW)

1 devices
1–1 of 1
No devices found for this product code.

About Product Code NLW - Regulatory Context