Medical Device Manufacturer · US , Columbia , MO

Neal & Assoc., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Neal & Assoc., Inc. has 2 FDA 510(k) cleared medical devices. Based in Columbia, US.

Historical record: 2 cleared submissions from 1988 to 1993. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Neal & Assoc., Inc. Filter by specialty or product code using the sidebar.

Neal & Assoc., Inc. 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 - Neal & Assoc., Inc.

2 devices

1-2 of 2