Medical Device Manufacturer · US , Elizabeth , CO

Access Battery, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

Access Battery, Inc. has 2 FDA 510(k) cleared medical devices. Based in Elizabeth, US.

Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Obstetrics & Gynecology.

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

Access Battery, 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 - Access Battery, Inc.

2 devices

1-2 of 2