Medical Device Manufacturer · US , Mchenry , IL

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

17 submissions · 16 cleared · Since 1982

17

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interspec, Inc. Neurology ✕

2 devices

1-2 of 2

Cleared Apr 30, 1984

Neurology · 76d

Cleared Dec 07, 1982

Neurology · 47d