Medical Device Manufacturer · US , Beverly , MA

Eurospital - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Eurospital has 1 FDA 510(k) cleared medical devices. Based in Beverly, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General Hospital.

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Eurospital is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eurospital

1 devices

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