Medical Device Manufacturer · US , Riviera Beach , FL

Smith-Perry Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989
2
Total
2
Cleared
0
Denied

Smith-Perry Corp. has 2 FDA 510(k) cleared medical devices. Based in Riviera Beach, US.

Historical record: 2 cleared submissions from 1989 to 1990. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Smith-Perry Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Smith-Perry Corp.
2 devices
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