Medical Device Manufacturer · US , Mchenry , IL

Genetic - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1983

Official Website

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Genetic Cardiovascular ✕

1 devices

1-1 of 1

Cleared Dec 26, 1983

PERI-GUARD PERICARDIAL PATCH-HERNIA

Cardiovascular · 111d