Medical Device Manufacturer · US , Lake Park , FL

Anspach Mfg., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1991

Total

Cleared

Denied

Anspach Mfg., Inc. has 3 FDA 510(k) cleared medical devices. Based in Lake Park, US.

Historical record: 3 cleared submissions from 1991 to 1994. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Anspach Mfg., Inc.

3 devices

1-3 of 3