KTD · Class I · 21 CFR 890.3490

FDA Product Code KTD: Orthosis, Abdominal

3
Total
3
Cleared
22d
Avg days
1978
Since

FDA 510(k) Cleared Orthosis, Abdominal Devices (Product Code KTD)

3 devices
1–3 of 3
No devices found for this product code.

About Product Code KTD - Regulatory Context