Medical Device Manufacturer · CH , Baar

Schiller AG - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1985

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Schiller AG Anesthesiology ✕

2 devices

1-2 of 2

Cleared May 12, 2000

SPIROVIT SP-2, PNEUMOCHECK II

Anesthesiology · 263d

Cleared Apr 30, 1999

SPIROVIT, MODEL SP-250

Anesthesiology · 169d