Medical Device Manufacturer · US , Mchenry , IL

A&A Ent. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1977

Total

Cleared

Denied

A&A Ent. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1977 to 1977. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by A&A Ent. Filter by specialty or product code using the sidebar.

A&A Ent. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - A&A Ent.

2 devices

1-2 of 2