Cherry Plastics, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cherry Plastics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1984 to 1984. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Cherry Plastics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cherry Plastics, Inc.
2 devices