Medical Device Manufacturer · US , Mountain View , CA

Siegen Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1984

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Siegen Corp. Neurology ✕

6 devices

1-6 of 6

Cleared Oct 01, 1987

SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.

Neurology · 134d

Cleared Oct 14, 1986

NEUROSCOPE SEEG

Neurology · 152d

Cleared Sep 26, 1986

SIEGEN HEADPHONES

Neurology · 92d

Cleared Feb 14, 1985

SIEGEN VISUAL STIMULATOR

Neurology · 79d

Cleared Dec 11, 1984

SIEGEN SURFACE ELECTRODES

Neurology · 12d

Cleared Nov 20, 1984

SIEGEN NEUROSCOPE

Neurology · 76d