Medical Device Manufacturer · AU , Sydney, Australia

Nascor Pty. , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

Total

Cleared

Denied

Nascor Pty. , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Sydney, Australia, AU.

Historical record: 2 cleared submissions from 1991 to 1994. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Nascor Pty. , Ltd. Filter by specialty or product code using the sidebar.

Nascor Pty. , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nascor Pty. , Ltd.

2 devices

1-2 of 2