Medical Device Manufacturer · US , Tarpon Springs , FL

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

2 submissions · 2 cleared · Since 1995

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Msi, Inc. Toxicology ✕

1 devices

1-1 of 1

Cleared Jun 21, 1995

MSI PROCEDURE KIT

Toxicology · 295d