Medical Device Manufacturer · US , Grand Island , NY

Invitrogen Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Invitrogen Corporation Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Dec 23, 2002

AIM-V (R) MEDIUM, MODEL 087-0112

Gastroenterology & Urology · 179d