LJK · Class II · 21 CFR 866.3780

FDA Product Code LJK: Antisera, If, Toxoplasma Gondii

6
Total
6
Cleared
97d
Avg days
1982
Since

FDA 510(k) Cleared Antisera, If, Toxoplasma Gondii Devices (Product Code LJK)

6 devices
1–6 of 6
No devices found for this product code.

About Product Code LJK - Regulatory Context