JEL · Class II · 21 CFR 874.4680

FDA Product Code JEL: Curette, Biopsy, Bronchoscope (rigid)

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).

1
Total
1
Cleared
257d
Avg days
1994
Since

FDA 510(k) Cleared Curette, Biopsy, Bronchoscope (rigid) Devices (Product Code JEL)

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

About Product Code JEL - Regulatory Context