Medical Device Manufacturer · US , Dayton , OH

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

2 submissions · 2 cleared · Since 1986

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Versacor, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Jan 27, 1986

CUSTO PORT 24-H ECG AMBULATORY RECORDER

Cardiovascular · 111d