Medical Device Manufacturer · US , Mchenry , IL

Verimed Holdings, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1983

12

Total

12

Cleared

0

Denied

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

6 devices

1-6 of 6

Cleared Nov 14, 1995

BIOFEEDBACK DEVICE

Neurology · 75d

Cleared Jun 14, 1995

MYOEXORCISER II FUAL

Neurology · 48d

Cleared Dec 10, 1992

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)

Neurology · 195d

Cleared Dec 13, 1989

VERIMED MYOEXORCISER III (MYO III)

Neurology · 245d

Cleared Jan 21, 1986

Neurology · 193d

Cleared Oct 28, 1983

VERIMED MYOEXORCISER

Neurology · 77d