Access Battery, Inc. is one of 25774 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Access Battery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BATTERY PACK, RECHARGEABLE, MODELS MLA0051, MLA90479, MNC5169L/P, MNC1000EKG, MNC14649P, BATTERY, RECHARGEABLE
2
Total
2
Cleared
0
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.
FDA 510(k) Regulatory Record - Access Battery, Inc.
2 devices