Sherwood Medical Industries - FDA 510(k) Cleared Devices
Recent clearances: SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES, LANCER GLUCOSE RATE REAGENT KIT, LANCER L-INA HUMAN REFERENCE SERUM
62
Total
62
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sherwood Medical Industries Cardiovascular ✕
4 devices