Medical Device Manufacturer · US , Washington , DC

Medtech , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Recent clearances: INTROMIT HAND ACCESS PORT FOR HAND ASSISTED LAPAROSCOPIC SURGERY, MODEL FP880-150

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Medtech , Ltd. General & Plastic Surgery ✕

1 devices
1-1 of 1
Filters