Medical Device Manufacturer · US , Miami , FL

Angi-Pak Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Angi-Pak Corp. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Sep 29, 1986

CORDIPAK CARDIAC CATHETERIZATION PACK

Cardiovascular · 32d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 28, 2026