Medical Device Manufacturer · KR , Seoul

Spass, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Spass, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Jun 15, 2023

Cardiovascular · 121d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 17, 2026