Medical Device Manufacturer · US , Coon Rapids , MN

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

3 submissions · 3 cleared · Since 1986

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Endotronics, Inc. Pathology ✕

3 devices

1-3 of 3

Cleared Jan 12, 1988

Pathology · 28d

Cleared Jun 15, 1987

Pathology · 14d

Cleared Nov 24, 1986

ACUSYST-P (CELL CULTURE EQUIPMENT)

Pathology · 20d