Medical Device Manufacturer · US , Wood Dale , IL

Stoelting Co. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1995

Recent clearances: MODIFICATION TO A620 EEG, AT 62 EEG (A.K.A THE A, AT53 DUAL CHANNEL EMG

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Stoelting Co. Neurology ✕

4 devices

1-4 of 4

Cleared Oct 10, 2001

MODIFICATION TO A620 EEG

Neurology · 104d

Cleared Feb 05, 1997

AT 62 EEG (A.K.A THE A

Neurology · 51d

Cleared Apr 17, 1996

AT53 DUAL CHANNEL EMG

Neurology · 303d

Cleared Sep 18, 1995

Neurology · 363d