Medical Device Manufacturer · US , Washington , DC

Seidel Medizin GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Seidel Medizin GmbH Anesthesiology ✕

2 devices

1-2 of 2

Cleared May 16, 1996

LARKEL DEVICE WITH ATTACHMENTS A-H(MODIFICATION)

Anesthesiology · 331d

Cleared Sep 16, 1987

LARKEL DEVICE W/ATTACHMENTS A-H

Anesthesiology · 85d